What Moves the Needle
A letter earned on deaths, heart attacks or fractures is a different kind of evidence from a letter earned on a blood test. This page puts every graded use on EBL in order of what its trials actually measured, strongest kind of outcome first. It ranks evidence. It does not tell you what to do.
526 graded uses across supplements, protocols, devices and longevity drugs. A record graded for several uses appears once for each. Each row opens its record and its trials.
On deaths and disease events, each row also gives the absolute size: out of 1,000 people (or 1,000 person-years), how many had the event in the comparison group and how many with the treatment, as the trial's abstract states it, with the outcome, the people, the comparison and the time it belongs to. Within each letter, rows are listed by name.
Each figure answers a different question, about a different outcome, group of people, comparison and length of time. The numbers cannot be compared with each other.
Measured on deaths and disease events
Heart attacks, strokes, fractures, cancers, deaths, infections: things that happen to people and are counted. A 17 · B 14 · C 30.
- AHard clinical endpointIntensive systolic target (under 120 to 130 mm Hg) against a standard target: major cardiovascular events · Protocol5.4 fewer per 1,000 person-years, over a median 3.26 years. Outcome: major cardiovascular events (counted once: the first heart attack, other acute coronary syndrome, stroke, heart failure or cardiovascular death). In: 9,361 adults with systolic pressure of 130 or higher and raised cardiovascular risk, without diabetes (SPRINT). Compared: systolic target under 120 against under 140 mm Hg. 21.9 in the comparison group against 16.5 with the treatment. PMID PubMed ID: the permanent number the US National Library of Medicine gives a published paper. Each one links to that paper's record on PubMed. 26551272.
- AHard clinical endpointLowering blood pressure in people with high blood pressure, against placebo An inactive substitute made to look like the real treatment, so participants cannot tell which one they received. or less treatment: major cardiovascular events and death · Protocol6 fewer per 1,000 person-years, over a median 4.15 years. Outcome: major cardiovascular events (counted once: the first stroke, heart attack or ischemic heart disease, or heart failure causing death or a hospital stay). In: 186,988 people without previous cardiovascular disease, 48 trials. Compared: blood-pressure-lowering drugs against placebo, other drugs or less intensive treatment. 31.9 in the comparison group against 25.9 with the treatment. In people with previous cardiovascular disease the same review gives 39.7 against 36.0 per 1,000 person-years. PMID 33933205.
- AHard clinical endpointRecurrent C. difficile infection, adults · Protocol333 more per 1,000 people, per treatment course. Outcome: recurrent C. difficile infection resolved. In: 320 adults with recurrent C. difficile infection, 6 trials. Compared: donor stool transplant against placebo, own-stool transplant, no treatment or antibiotics (mostly vancomycin). How it was obtained: computed from the number needed to treat the abstract states, 3. PMID 37096495.
- AHard clinical endpointHeart attack, stroke and cardiovascular death, lowering LDL Low-density lipoprotein cholesterol, the cholesterol fraction most closely tied to plaque in the arteries. cholesterol in people without vascular disease who are at raised risk · Protocol25 fewer per 1,000 people, over about 5 years. Outcome: major vascular events (counted once: the first heart attack or coronary death, coronary revascularization or stroke). In: people without coronary heart disease, in 14 statin trials of 90,056 people. Compared: statin against control, scaled to 1 mmol/L lower LDL cholesterol. How it was obtained: stated in the abstract: 25 fewer per 1,000 among those with no such history. PMID 16214597.
- AHard clinical endpointHeart attack, stroke and death, lowering LDL cholesterol in people with established vascular disease or after an acute coronary syndrome · Protocol48 fewer per 1,000 people, over about 5 years. Outcome: major vascular events (counted once: the first heart attack or coronary death, coronary revascularization or stroke). In: people with coronary heart disease, in 14 statin trials of 90,056 people. Compared: statin against control, scaled to 1 mmol/L lower LDL cholesterol. How it was obtained: stated in the abstract: 48 fewer per 1,000 among those with coronary heart disease. PMID 16214597.
- AHard clinical endpointLung cancer deaths, current and former heavy smokers aged 50 to 74 · Device or therapy0.6 fewer per 1,000 person-years, during the trial. Outcome: death from lung cancer. In: 53,454 current and former heavy smokers (NLST). Compared: three yearly low-dose CT scans against three yearly chest X-rays. 3.1 in the comparison group against 2.5 with the treatment. PMID 21714641.
- AHard clinical endpointMajor cardiovascular events (PREDIMED) · Protocol6 fewer per 1,000 people, over a median 4.8 years. Outcome: major cardiovascular events (counted once: the first heart attack, stroke or cardiovascular death). In: 7,447 adults aged 55 to 80 at high cardiovascular risk, without cardiovascular disease, Spain (PREDIMED). Compared: Mediterranean diet with extra-virgin olive oil against advice to cut dietary fat. 44 in the comparison group against 38 with the treatment. PMID 29897866.
- AHard clinical endpointVenous thromboembolism prevention · Protocol94 fewer per 1,000 people, during the hospital stay. Outcome: deep vein thrombosis. In: 16,164 hospitalized patients, 70 trials. Compared: intermittent pneumatic compression against no compression. 167 in the comparison group against 73 with the treatment. PMID 23852609.
- AHard clinical endpointRSV lung illness and RSV hospitalization, bivalent RSV prefusion F vaccine, adults aged 60 and older · Protocol0.6 fewer per 1,000 person-years, over one winter. Outcome: hospitalization for RSV respiratory disease. In: 131,276 adults aged 60 and older in Denmark (DAN-RSV). Compared: one dose of bivalent RSV prefusion F vaccine against no vaccine. 0.7 in the comparison group against 0.1 with the treatment. PMID 40888695.
- AHard clinical endpointCardiovascular death, heart attack and stroke in people with cardiovascular disease or type 2 diabetes · Longevity drug15 fewer per 1,000 people, over a mean 39.8 months. Outcome: major adverse cardiovascular events (counted once: the first cardiovascular death, nonfatal heart attack or nonfatal stroke). In: 17,604 adults aged 45 and over with cardiovascular disease and overweight or obesity, without diabetes (SELECT). Compared: semaglutide 2.4 mg weekly against placebo. 80 in the comparison group against 65 with the treatment. PMID 37952131.
- AHard clinical endpointCardiovascular death, heart-failure hospitalization and kidney-failure progression · Longevity drug49 fewer per 1,000 people, over a median 18.2 months. Outcome: worsening heart failure or cardiovascular death (counted once: the first hospital stay or urgent visit for heart failure, or cardiovascular death). In: 4,744 adults with heart failure and an ejection fraction of 40% or less (DAPA-HF). Compared: dapagliflozin 10 mg daily against placebo, both added to standard therapy. 212 in the comparison group against 163 with the treatment. Kidney failure is a separate outcome and is not in this number. PMID 31535829.
- AHard clinical endpointShingles (herpes zoster) in adults aged 50 and older · Protocol8.8 fewer per 1,000 person-years, over a mean 3.2 years. Outcome: shingles (herpes zoster). In: 15,411 adults aged 50 and over in 18 countries (ZOE-50). Compared: two doses of recombinant zoster vaccine against placebo. 9.1 in the comparison group against 0.3 with the treatment. PMID 25916341.
- AHard clinical endpointColorectal cancer deaths, an invitation to flexible sigmoidoscopy, adults aged 55 to 64 · Device or therapy1.3 fewer per 1,000 people, over 15 years. Outcome: death from colorectal cancer. In: 274,952 adults aged 55 to 64, 4 trials. Compared: invitation to sigmoidoscopy screening against usual care. How it was obtained: stated in the abstract: 0.13 fewer deaths per 100 people invited. PMID 36215714.
- AHard clinical endpointDeath and major cardiovascular events in people with coronary heart disease or other established vascular disease · Longevity drug37 fewer per 1,000 people, over 6 years. Outcome: death from any cause. In: 4,444 adults with coronary heart disease and high cholesterol (4S). Compared: simvastatin against placebo. 124 in the comparison group against 87 with the treatment. PMID 7968073.
- AHard clinical endpointHeart attack, stroke and cardiovascular death in people without cardiovascular disease who are at raised risk · Longevity drug5.9 fewer per 1,000 person-years, over a median 1.9 years. Outcome: major cardiovascular events (counted once: the first heart attack, stroke, artery-opening procedure, hospital stay for unstable angina or cardiovascular death). In: 17,802 healthy adults with LDL under 130 mg/dL and raised C-reactive protein (JUPITER). Compared: rosuvastatin 20 mg daily against placebo. 13.6 in the comparison group against 7.7 with the treatment. PMID 18997196.
- AHard clinical endpointColorectal cancer mortality, guaiac FOBT (gFOBT) · Device or therapyAbsolute size: not stated in the abstract (PMID 24047060). The abstract gives colorectal-cancer deaths as a share of all deaths, not of the people screened.
- AHard clinical endpointFewer cavities, fluoride toothpaste in children and adolescents · ProtocolAbsolute size: not stated in the abstract (PMID 12535435). The outcome is the number of decayed, missing or filled tooth surfaces per child, a count rather than an event, so it has no rate per 1,000 people.
- BHard clinical endpointDementia or mild cognitive impairment · Protocol1.4 fewer per 1,000 person-years, over a median 5.11 years. Outcome: probable dementia. In: 9,361 adults aged 50 and over with high blood pressure, without diabetes or stroke (SPRINT MIND). Compared: systolic target under 120 against under 140 mm Hg. 8.6 in the comparison group against 7.2 with the treatment. Not statistically significant Unlikely to be explained by chance alone at the threshold the study set. It says nothing about whether the difference is large enough to matter. on its own. PMID 30688979.
- BHard clinical endpointChronic heart failure events, including hospitalization, as an adjunct A treatment tested on top of standard prescribed therapy rather than in place of it. to standard therapy · Supplement110 fewer per 1,000 people, over 2 years. Outcome: major adverse cardiovascular events, the trial's long-term combined endpoint The outcome a trial measures to decide whether the treatment worked, such as heart attacks, blood pressure or a symptom score. (counted once: the first such event). In: 420 adults with moderate to severe chronic heart failure on standard therapy (Q-SYMBIO). Compared: CoQ10 100 mg three times a day against placebo, both added to standard therapy. 260 in the comparison group against 150 with the treatment. PMID 25282031.
- BHard clinical endpointHeart-failure events, including hospitalization, in chronic heart failure · Protocol110 fewer per 1,000 people, over 2 years. Outcome: major adverse cardiovascular events, the trial's long-term combined endpoint (counted once: the first such event). In: 420 adults with moderate to severe chronic heart failure on standard therapy (Q-SYMBIO). Compared: CoQ10 100 mg three times a day against placebo, both added to standard therapy. 260 in the comparison group against 150 with the treatment. PMID 25282031.
- BHard clinical endpointFirst-stroke prevention in hypertensive adults without prior stroke or MI, in populations without grain folate fortification (0.8 mg/day with enalapril) · Supplement7 fewer per 1,000 people, over a median 4.5 years. Outcome: first stroke. In: 20,702 adults with high blood pressure and no earlier stroke or heart attack, China (CSPPT). Compared: enalapril with folic acid 0.8 mg against enalapril alone. 34 in the comparison group against 27 with the treatment. PMID 25771069.
- BHard clinical endpointInvasive cervical cancer, HPV-based against cytology-based screening, women aged 20 to 64 · Device or therapyAbsolute size: not stated in the abstract (PMID 24192252). The abstract gives a rate ratio for all women; its per-100,000 figures cover only women who tested negative at entry.
- BHard clinical endpointMajor cardiovascular events, high-dose icosapent ethyl in statin-treated people with raised triglycerides · Protocol48 fewer per 1,000 people, over a median 4.9 years. Outcome: major adverse cardiovascular events (counted once: the first cardiovascular death, heart attack, stroke, coronary revascularization or unstable angina). In: 8,179 adults on a statin with cardiovascular disease, or diabetes and other risk factors, and raised triglycerides (REDUCE-IT). Compared: icosapent ethyl 4 g a day against placebo. 220 in the comparison group against 172 with the treatment. PMID 30415628.
- BHard clinical endpointBreast cancer deaths, women aged 50 to 69 · Device or therapy0.8 fewer per 1,000 people, over 10 years. Outcome: death from breast cancer. In: women aged 50 to 59, 7 trials. Compared: mammography screening against no screening. At ages 60 to 69 the same review gives 21 fewer per 10,000, which is 2.1 per 1,000. How it was obtained: stated in the abstract: 8 and 21 deaths prevented per 10,000 women at 50 to 59 and 60 to 69. PMID 26756588.
- BHard clinical endpointMajor adverse cardiovascular events, high-dose icosapent ethyl · Supplement48 fewer per 1,000 people, over a median 4.9 years. Outcome: major adverse cardiovascular events (counted once: the first cardiovascular death, heart attack, stroke, coronary revascularization or unstable angina). In: 8,179 adults on a statin with cardiovascular disease, or diabetes and other risk factors, and raised triglycerides (REDUCE-IT). Compared: icosapent ethyl 4 g a day against placebo. 220 in the comparison group against 172 with the treatment. PMID 30415628.
- BHard clinical endpointInvasive pneumococcal disease, 23-valent polysaccharide vaccine, adults · ProtocolAbsolute size: not stated in the abstract (PMID 23440780). The abstract gives a pooled odds ratio (0.26) without the number of cases in each group.
- BHard clinical endpointProstate cancer deaths, men aged 55 to 69 · Device or therapy1.8 fewer per 1,000 people, at 16 years. Outcome: death from prostate cancer. In: men aged 55 to 69 in eight European countries (ERSPC). Compared: invitation to PSA screening against no invitation. How it was obtained: stated in the abstract: an absolute difference of 0.18 percent at 16 years. PMID 30824296.
- BHard clinical endpointMajor cardiovascular events in adults aged 70 and over without cardiovascular disease · Longevity drug4.6 fewer per 1,000 person-years, over a median 5.9 years. Outcome: major cardiovascular events (counted once: the first cardiovascular death, nonfatal heart attack or stroke, or coronary revascularization). In: 9,971 adults aged 70 and over without cardiovascular disease, diabetes or dementia, Australia (STAREE). Compared: atorvastatin 40 mg daily against placebo. 15.5 in the comparison group against 10.9 with the treatment. PMID 42670961.
- BHard clinical endpointDisease-free survival and overall survival after curative-intent treatment for non-metastatic cancer, structured exercise program against health education or usual care · Protocol64 fewer per 1,000 people, at 5 years. Outcome: disease-free survival events (counted once: the first cancer recurrence, new cancer or death). In: 889 adults with resected colon cancer who had finished chemotherapy (CHALLENGE). Compared: a 3-year structured exercise program against health-education materials. 261 in the comparison group against 197 with the treatment. Overall survival is a separate outcome and is not in this number. PMID 40450658.
- BHard clinical endpointFewer cavities, fluoride toothpaste in adults · ProtocolAbsolute size: not stated in the abstract (PMID 30829399). The outcome is the number of decayed, missing or filled tooth surfaces per person, a count rather than an event, so it has no rate per 1,000 people.
- BHard clinical endpointFracture prevention, vitamin D3 with calcium, older adults living in institutions · Supplement9 fewer per 1,000 people, per year. Outcome: hip fracture. In: older adults living in institutions (pooled trials of vitamin D with calcium). Compared: vitamin D with calcium against placebo or no treatment. 54 in the comparison group against 45 with the treatment. How it was obtained: stated in the abstract: nine fewer per 1,000 per year in institutions. PMID 24729336.
- CHard clinical endpointProgression from impaired glucose tolerance to type 2 diabetes · Longevity drug100 fewer per 1,000 people, during the trial. Outcome: type 2 diabetes diagnosed. In: 1,368 adults with impaired glucose tolerance (STOP-NIDDM). Compared: acarbose 100 mg three times a day against placebo. 420 in the comparison group against 320 with the treatment. PMID 12086760.
- CHard clinical endpointAll-cause mortality in middle-aged men with heavy drinking, screening with an intervention to drink less · ProtocolAbsolute size: not stated in the abstract (PMID 6135365). The abstract gives a relative reduction only (mortality by 50 percent), with no number of deaths in each group.
- CHard clinical endpointAtrial fibrillation recurrence in regular drinkers with AF · Protocol200 fewer per 1,000 people, over 6 months. Outcome: atrial fibrillation recurrence. In: 140 adults with atrial fibrillation who drank 10 or more drinks a week, Australia. Compared: stopping alcohol against usual drinking. 730 in the comparison group against 530 with the treatment. PMID 31893513.
- CHard clinical endpointTreating high blood pressure in adults aged 80 and over · ProtocolAbsolute size: not stated in the abstract (PMID 18378519). The abstract gives reductions as percentages only (death from any cause 21 percent lower), with no rate in each group.
- CHard clinical endpointHeart and circulation events and fractures after a 12-week pedometer walking program, adults aged 45 to 75 · Protocol16 fewer per 1,000 people, over 4 years after a 12-week program. Outcome: cardiovascular events (counted once: the first nonfatal or fatal cardiovascular event). In: 1,297 adults aged 45 to 75 in UK general practices, two trials (PACE-UP and PACE-Lift). Compared: a 12-week pedometer walking program against usual care. Fractures are a separate outcome: 36 fewer per 1,000 in the same abstract. How it was obtained: absolute risk The actual chance of an event in a group. A fall from 2 percent to 1 percent is a 1-point absolute reduction, even though it is a 50 percent relative one. reduction stated in the abstract (1.6%, number needed to treat 61); the abstract gives no group rates. PMID 31237875.
- CHard clinical endpointCervical cancer deaths, one round of HPV testing against standard care, women aged 30 to 59 in rural India · Device or therapy1 fewer per 1,000 people, during the trial. Outcome: death from cervical cancer. In: 131,746 women aged 30 to 59 in rural India, cluster trial. Compared: one round of HPV testing against standard care. 2 in the comparison group against 1 with the treatment. How it was obtained: computed from the deaths and group sizes in the abstract: 34 of 34,126 against 64 of 31,488. PMID 19339719.
- CHard clinical endpointLaboratory-confirmed influenza, high-dose against standard-dose vaccine, adults aged 65 and older · Protocol5 fewer per 1,000 people, over two influenza seasons, intention to treat. Outcome: laboratory-confirmed influenza with a protocol-defined illness. In: 31,989 adults aged 65 and older in the United States and Canada. Compared: high-dose against standard-dose inactivated influenza vaccine. 19 in the comparison group against 14 with the treatment. How it was obtained: group percentages in the abstract (1.9% and 1.4%). PMID 25119609.
- CHard clinical endpointDeath from any cause, current and former heavy smokers · Device or therapyAbsolute size: not stated in the abstract (PMID 21714641). The abstract gives the reduction in deaths from any cause as a percentage only (6.7 percent lower), with no death rate in each group.
- CHard clinical endpointCOPD exacerbation rate at 600 mg twice daily in moderate to severe COPD · Supplement330 fewer per 1,000 person-years, over 1 year. Outcome: COPD exacerbations (counted as events per person-year). In: 1,006 adults aged 40 to 80 with moderate to severe COPD, China (PANTHEON). Compared: NAC 600 mg twice a day against placebo. 1,490 in the comparison group against 1,160 with the treatment. PMID 24621680.
- CHard clinical endpointOvulation and pregnancy in clomiphene-resistant polycystic ovary syndrome, NAC added to clomiphene · Supplement213 more per 1,000 people, per treatment course. Outcome: pregnancy. In: 150 women aged 18 to 39 with clomiphene-resistant polycystic ovary syndrome. Compared: NAC 1.2 g a day with clomiphene against placebo with clomiphene. 0 in the comparison group against 213 with the treatment. PMID 15705376.
- CHard clinical endpointCardiovascular events, including coronary death · ProtocolAbsolute size: not stated in the abstract (PMID 31567003). The pooled analysis gives rate ratios only, with no event rate in each group.
- CHard clinical endpointSecondary prevention after myocardial infarction · SupplementAbsolute size: not stated in the abstract (PMID 10465168). The abstract gives relative reductions only (death 14 percent lower), with no event rate in each group.
- CHard clinical endpointPneumonia from the vaccine's strains, 13-valent conjugate vaccine, adults aged 65 and older · ProtocolAbsolute size: not stated in the abstract (PMID 25785969). The abstract gives the number of cases in each group (49 and 90) but not the per-protocol group sizes, so a rate per 1,000 cannot be computed from it.
- CHard clinical endpointPrevention of antibiotic-associated C. difficile diarrhea (people taking antibiotics who are not immunocompromised) · Supplement16 fewer per 1,000 people, during a course of antibiotics. Outcome: C. difficile-associated diarrhea. In: 13,179 adults and children taking antibiotics, 38 trials. Compared: probiotics against placebo, no treatment or other prevention. 32 in the comparison group against 16 with the treatment. PMID 40931979.
- CHard clinical endpointDeath from any cause, a quit-smoking program, middle-aged smokers · Protocol1.6 fewer per 1,000 person-years, over up to 14.5 years. Outcome: death from any cause. In: 5,887 middle-aged smokers with mild airway obstruction (Lung Health Study). Compared: a 10-week quit-smoking program against usual care. 10.4 in the comparison group against 8.8 with the treatment. PMID 15710956.
- CHard clinical endpointSecondary prevention after myocardial infarction · Supplement47 fewer per 1,000 people, over an average 4.5 years. Outcome: major coronary events (counted once: the first nonfatal heart attack or death from coronary heart disease). In: nearly 5,000 Chinese adults after a heart attack (CCSPS). Compared: Xuezhikang, a red yeast rice extract, against placebo. 104 in the comparison group against 57 with the treatment. PMID 18549841.
- CHard clinical endpointRSV lung illness, adjuvanted RSVPreF3 vaccine, adults aged 60 and older · Protocol4.8 fewer per 1,000 person-years, over a median 6.7 months. Outcome: RT-PCR-confirmed RSV lower respiratory tract disease. In: 24,966 adults aged 60 and older. Compared: adjuvanted RSVPreF3 vaccine against placebo. 5.8 in the comparison group against 1 with the treatment. PMID 36791160.
- CHard clinical endpointRSV lung illness, mRNA-1345 vaccine, adults aged 60 and older · ProtocolAbsolute size: not stated in the abstract (PMID 38091530). The abstract gives vaccine efficacy (83.7%) and group sizes but not the number of cases in each group.
- CHard clinical endpointCoronary and cardiovascular events when linoleic-acid oils replace saturated fat · ProtocolAbsolute size: not stated in the abstract (PMID 20351774). The pooled analysis gives a relative risk The risk in one group expressed as a share of the risk in another. It can make a small absolute difference look large. only (19 percent lower), with no event rate in each group.
- CHard clinical endpointColorectal cancer diagnoses, an invitation to screening colonoscopy, adults aged 55 to 64 · Device or therapy2.2 fewer per 1,000 people, at 10 years. Outcome: colorectal cancer diagnosed. In: 84,585 adults aged 55 to 64 in Poland, Norway and Sweden (NordICC). Compared: invitation to one screening colonoscopy against no invitation. 12 in the comparison group against 9.8 with the treatment. PMID 36214590.
- CHard clinical endpointMortality in lonely older adults, psychosocial group rehabilitation · Protocol70 fewer per 1,000 people, over 2 years. Outcome: death from any cause. In: 235 lonely adults over 74 at seven day-care centers. Compared: 12 psychosocial group sessions over 3 months against a control group without them. 100 in the comparison group against 30 with the treatment. PMID 19223606.
- CHard clinical endpointColorectal cancer mortality versus colonoscopy · Device or therapy0.2 more per 1,000 people, over 10 years. Outcome: death from colorectal cancer. In: adults aged 50 to 69 at average risk, Spain (COLONPREV). Compared: invitation to a stool test (FIT) every 2 years against invitation to one colonoscopy. 2.2 in the comparison group against 2.4 with the treatment. PMID 40158525.
- CHard clinical endpointMelanoma, daily sunscreen · ProtocolAbsolute size: not stated in the abstract (PMID 21135266). The abstract gives the number of melanomas in each group (11 against 22) but not the size of each group.
- CHard clinical endpointOral nicotinamide, new keratinocyte skin cancers in people with prior skin cancer (not immunosuppressed) · ProtocolAbsolute size: not stated in the abstract (PMID 26488693). The abstract gives the reduction as a percentage only (23 percent fewer new cancers), with no rate in each group.
- CHard clinical endpointSquamous cell carcinoma of the skin, daily sunscreen · ProtocolAbsolute size: not stated in the abstract (PMID 10475183). The abstract's per-100,000 figures count tumors, not people, and the number of people with a first new squamous cell cancer did not differ significantly.
- CHard clinical endpointPneumonia in nursing home residents, professional oral care · ProtocolAbsolute size: not stated in the abstract (PMID 11943036). The abstract reports that pneumonia decreased but gives no number of cases in either group.
- CHard clinical endpointOnset of type 2 diabetes in obesity with prediabetes · Longevity drug120 fewer per 1,000 people, over 176 weeks. Outcome: onset of type 2 diabetes. In: 1,032 adults with obesity and prediabetes (SURMOUNT-1). Compared: tirzepatide 5 to 15 mg weekly against placebo. 133 in the comparison group against 13 with the treatment. PMID 39536238.
- CHard clinical endpointDeath, heart attack and stroke in coronary heart disease · ProtocolAbsolute size: not stated in the abstract (PMID 23149426). The abstract gives a hazard ratio How often an event happened in the treated group compared with the control group over the same period. A ratio of 0.80 means 20 percent fewer events. only (48 percent lower), with no event rate in each group.
- CHard clinical endpointOverall survival after curative resection of colorectal or gastric cancer, PSK added to chemotherapy · SupplementAbsolute size: not stated in the abstract (PMID 16133112). The abstract gives a survival risk ratio only, with no death rate in each group.
- CHard clinical endpointPrevention of acute respiratory tract infection (esp. in vitamin D-deficient people) · SupplementAbsolute size: not stated in the abstract (PMID 28202713). The abstract gives odds ratios only, with no infection rate in each group.
Measured on function
Strength, walking, balance, wakefulness: what a person can do, measured with an instrument. A 12 · B 10 · C 58.
- AMeasured functionStrength gains (one-repetition maximum) during resistance training, healthy adults · Protocol
- AMeasured functionMeasured VO2max The most oxygen the body can use during all-out exercise, a standard measure of aerobic fitness. after low-to-moderate intensity aerobic training, against no exercise · Protocol
- AMeasured functionDaytime sleepiness measured by the maintenance of wakefulness test, in moderate to severe sleep apnea with daytime sleepiness · Device or therapy
- AMeasured functionMuscle strength with resistance training in older adults · Supplement
- AMeasured functionAlertness and cognitive performance in the hours after an afternoon nap, healthy adults · Protocol
- AMeasured functionCognitive performance during a night shift after an on-shift nap · Protocol
- AMeasured functionMemory retention after an afternoon nap · Protocol
- AMeasured functionMeasured VO2max rises more with a larger weekly exercise amount, in inactive middle-aged and older adults · Protocol
- AMeasured functionEarly quadriceps strength and mobility after total knee replacement, compared with usual care (dynamometer strength, timed up-and-go) · Device or therapy
- AMeasured functionMuscle size and strength, progressive overload · Protocol
- A
- AVO2max (cardiorespiratory fitness), an objective functional measure · Device or therapy
- B
- BMeasured functionPost-ACL reconstruction rehabilitation · Device or therapy
- BMeasured functionLower-body dynamic strength (1RM) and maximal aerobic capacity (VO2max) under concurrent training · Protocol
- BMeasured functionPhysical performance in athletes and physically active young men · Protocol
- BMeasured functionCognitive symptoms in mild to moderate dementia · Supplement
- B
- BMeasured functionClinical lymphedema, limb volume reduction · Protocol
- B
- BMeasured functionCardiorespiratory fitness (measured VO2max) in inactive adults, REHIT protocol · Device or therapy
- BMeasured functionMeasured eyesight, cataract surgery against waiting · Protocol
- CMeasured functionCognition in mild cognitive impairment and mild Alzheimer's disease, and diabetic neuropathy pain · Supplement
- CMeasured functionThe 150-minute weekly dose specifically, against other weekly volumes · Protocol
- CMeasured functionCognitive scores in diagnosed mild cognitive impairment, Alzheimer's disease or diabetes with cognitive decline · Supplement
- CMeasured functionObjective cognitive test performance · Protocol
- CMeasured functionSarcopenia Age-related loss of muscle mass and strength. / older adults · Device or therapy
- C
- CMeasured functionMemory and behavior in chronic cerebral disorders of the elderly · Supplement
- CMeasured functionExercise performance / VO2 surrogate measures · Supplement
- CMeasured functionObjectively measured memory and cognitive test performance · Protocol
- C
- CMeasured functionA short nap combined with caffeine for afternoon sleepiness · Protocol
- CMeasured functionReducing habitual napping in older adults: verbal memory over one year · Protocol
- CMeasured functionVerbal learning in mild cognitive impairment · Supplement
- CMeasured functionSleep onset latency and sleep quality after a warm bath or shower one to two hours before bed · Protocol
- CMeasured functionHair growth in androgenetic alopecia, plant-derived exosome formulation (scalp injection) · Device or therapy
- C
- CMeasured functionSpeech understanding measured in a listening test, adults aged 55 to 79 with mild to moderate hearing loss · Device or therapy
- CMeasured functionCognitive decline over 3 years in older adults with hearing loss at higher risk of decline · Protocol
- CMeasured functionMuscle mass and handgrip strength in adults with diagnosed sarcopenia · Supplement
- CMeasured functionMuscle mass and strength in adults over 50 without sarcopenia · Supplement
- C
- CMeasured functionWorking memory and reaction measures during acute cold or combat stress · Supplement
- CMeasured functionA cognitive score (HDS-R) in mild cognitive impairment · Protocol
- CMeasured functionCognitive test scores in older adults with mild cognitive impairment · Supplement
- CMeasured functionCognitive decline in mild cognitive impairment and Alzheimer's disease · Supplement
- CMeasured functionSleep in adults with high blood pressure taking beta-blockers · Supplement
- CMeasured functionSleep onset latency and sleep quality (primary sleep disorders) · Supplement
- CMeasured functionSleep onset and sleep efficiency at low doses (0.3 to 0.5 mg) · Protocol
- CMeasured function6-minute walk distance and physical function in diagnosed aging frailty · Device or therapy
- CMeasured functionMemory retrieval and contextual memory after a single oral dose of about 260 mg · Supplement
- CMeasured functionSleep time and efficiency in people with sleep disorders · Device or therapy
- CMeasured functionRecovery of muscle strength after strenuous exercise · Supplement
- C
- CMeasured functionDelayed sleep phase and late sleepers: sleep timing and daytime function · Protocol
- CMeasured functionDementia in care facilities: nighttime sleep with morning bright light · Protocol
- CMeasured functionInsomnia: sleep measured by actigraphy, polysomnography and questionnaires · Protocol
- CMeasured functionOlder adults without dementia: sleep with brighter morning or daytime indoor light · Protocol
- CMeasured functionRotating-shift nurses: daytime sleepiness and reaction time with brief morning light · Protocol
- CMeasured functionWhole-day bright ceiling light in group care homes: cognitive decline and daily function · Protocol
- CMeasured functionSix-minute walk distance in peripheral artery disease · Supplement
- CMeasured functionPain-free and maximum walking distance in intermittent claudication · Supplement
- CMeasured functionMemory and cognition in older adults, bovine-cortex phosphatidylserine (no longer sold) · Supplement
- CMeasured functionPhysical function in adults 60 and over, power versus traditional strength training · Protocol
- CMeasured functionCognitive test performance in middle-aged and older adults · Supplement
- CMeasured functionPhysical activity, physical tests and thinking tests, structured volunteering for older adults · Protocol
- C
- C
- C
- CMeasured functionRisky driving, measured by in-car sensors, after sleep extension education in young drivers · Device or therapy
- CMeasured functionSustained attention and reaction time, measured by test, after sleep extension in healthy young adults · Device or therapy
- CMeasured functionCognition and memory in older adults · Supplement
- C
- CMeasured functionVisible skin aging (photoaging), daily sunscreen · Protocol
- C
- CMeasured functionCognition (limited human evidence) · Device or therapy
- CMeasured functionCognition in mild cognitive impairment · Device or therapy
- CMeasured functionCognitive test performance in healthy adults and mixed clinical samples · Device or therapy
- CMeasured functionMuscle endurance, strength and mitochondrial markers, where the pre-registered primary endpoints The one outcome a trial names in advance as its main test. Results on other outcomes carry less weight. were missed · Supplement
Measured on symptoms
Pain, mood, sleep quality: rated by a blinded clinician or reported by the person. A 3 · B 22 · C 63.
- ABlinded clinician ratingSevere (grade 3 to 4) oral mucositis during head and neck radiotherapy or chemoradiation and stem cell transplant, graded by blinded clinicians · Device or therapy
- AResponse and remission in treatment-resistant major depression on blinded clinician-rated scales (HAM-D, MADRS) · Device or therapy
- ABlinded clinician ratingPostoperative cognitive dysfunction in older adults having major surgery · Device or therapy
- BSleep in adults with insomnia and anxiety, measured by a wrist sleep monitor (actigraphy) in one trial and self-reported in the pooled trials · Protocol
- B
- BDepression scores, response and remission in winter seasonal depression and non-seasonal major depression on clinician-rated scales (SIGH-SAD, HAM-D, MADRS) · Device or therapy
- BSelf-reportMuscle soreness and short-term recovery after strenuous exercise · Device or therapy
- B
- BSelf-reportSelf-rated daytime sleepiness (Epworth scale) in adults with obstructive sleep apnea · Device or therapy
- BChronic low back pain and disability, short term (self-report) · Device or therapy
- BSelf-rated hearing-related quality of life and everyday communication, adults with mild to moderate hearing loss · Device or therapy
- BSelf-reported anxiety, HRV biofeedback (resonance breathing) training · Device or therapy
- BSelf-reportSeizure frequency in children and adolescents with drug-resistant epilepsy · Protocol
- BSelf-reported anxiety, depression and pain · Protocol
- B
- BSelf-reported sleep quality · Protocol
- B
- BSelf-reportDaytime sleepiness and apnea-hypopnea index after two to four months of daily mouth and throat exercises · Protocol
- BSelf-reportChronic neck pain and chronic tendinopathy pain, low-level laser therapy · Device or therapy
- BSelf-reported meaning, purpose and distress, meaning-centered therapy (mostly people with cancer) · Protocol
- BSelf-reported symptoms of interstitial cystitis · Longevity drug
- BDepression symptom scales (HAM-D and similar) · Supplement
- BSelf-reportInsomnia: sleep onset, time awake after sleep onset and sleep efficiency, from sleep diaries · Protocol
- B
- B
- C
- C
- C
- CSelf-reported anxiety, sleep and pain; cognitive test scores · Device or therapy
- C
- C
- CSelf-reportKnee osteoarthritis pain and stiffness (WOMAC, VAS) · Supplement
- C
- CSelf-reportOsteoarthritis pain and function, chondroitin as generally sold · Supplement
- C
- CSickness absence from work (self-reported) · Device or therapy
- CSelf-reportMajor depressive disorder, as an adjunct to SSRI treatment · Supplement
- C
- CSelf-reportAcute shoulder or elbow tendon pain, gel applied to the skin · Supplement
- CSelf-reportComplex regional pain syndrome type I, cream applied to the skin · Supplement
- C
- CChronic plantar heel pain (plantar fasciitis), self-report · Device or therapy
- CKnee osteoarthritis joint-space narrowing and symptoms · Supplement
- CSelf-reportNext-day fatigue after experimental sleep restriction in healthy volunteers · Supplement
- C
- CSelf-reportKnee symptoms in adults with knee osteoarthritis or knee discomfort · Supplement
- CSelf-reportPhysical complaints and appetite in mild depression (inpatients) · Device or therapy
- CSelf-reported sleep quality · Protocol
- C
- CBlinded clinician ratingActive Crohn's disease, induction of response or remission · Longevity drug
- C
- C
- CSelf-reported insomnia severity in adults with poor sleep · Protocol
- C
- CBlinded clinician ratingPrevention of delirium in older hospitalized/medical-ward patients · Supplement
- CBlinded clinician ratingDelirium after noncardiac surgery in adults aged 65 and over · Device or therapy
- CSelf-reportSymptom score during acute exacerbation of COPD, as an adjunct to oxygen · Device or therapy
- CBlinded clinician ratingSymptoms in schizophrenia, as an adjunct to antipsychotic treatment · Supplement
- CSelf-reportErectile function in mild to moderate erectile dysfunction, Korean red ginseng · Supplement
- CSelf-reported osteoarthritis pain and function · Protocol
- CSelf-reportNonspecific low back pain, low-level laser therapy · Device or therapy
- C
- CBlinded clinician ratingUpper respiratory infections in healthy adults (Lacticaseibacillus rhamnosus CRL 1505 only) · Supplement
- CKnee osteoarthritis pain, self-reported, short term · Device or therapy
- CSelf-reported meaning and purpose, programs for older adults without serious illness · Protocol
- C
- C
- C
- CBlinded clinician ratingMajor depressive disorder, SAM-e as monotherapy · Supplement
- CDepressive symptoms and sleep problems, self-reported, after gradual sleep extension with sleep advice in adolescents · Device or therapy
- CSelf-reportSelf-rated loneliness in older adults · Protocol
- CSelf-reportADHD symptoms in children, added to methylphenidate · Supplement
- CBlinded clinician ratingBehavior scores in autism spectrum disorder · Supplement
- CBlinded clinician ratingDepression after cardiac procedures · Supplement
- CBlinded clinician ratingNegative symptoms of schizophrenia, added to antipsychotic treatment · Supplement
- CSelf-reportTemporomandibular disorder pain (mixed: pooled analysis favorable, sham-controlled trials null) · Device or therapy
- CSelf-reportChronic tension-type headache pain · Device or therapy
- CBlinded clinician ratingDepressive symptoms in major depression, clinic-administered · Device or therapy
- CBlinded clinician ratingDepressive symptoms in major depression, home-based · Device or therapy
- CSelf-reportFalls, expedited first-eye cataract surgery in women over 70 · Protocol
- CSelf-reportFalls, home safety program for people aged 75 and older with severe visual impairment · Protocol
- C
- C
- CBlinded clinician ratingPreventing complex regional pain syndrome after a wrist fracture · Supplement
- C
- CSelf-reportIncidence and duration of upper respiratory tract infections · Supplement
- C
- CBlinded clinician ratingSlowing progression to advanced age-related macular degeneration in people at high risk (zinc 80 mg with copper) · Supplement
Measured only on a blood marker or other surrogate
A lab value or scan moved. Whether the people who took it lived longer or better was not measured. A 0 · B 43 · C 94.
- BSurrogate biomarkerLean (fat-free) mass during resistance training, healthy adults · Protocol
- BSurrogate biomarkerBlood pressure in people with hypertension · Protocol
- BSurrogate biomarkerBlood pressure in people drinking more than two drinks a day · Protocol
- BSurrogate biomarkerLipid profile (LDL, triglycerides) · Supplement
- BSurrogate biomarkerCortisol and stress or anxiety scores in stressed adults · Supplement
- B
- BSurrogate biomarkerHbA1c A blood test that reflects average blood sugar over the previous two to three months. and LDL cholesterol in type 2 diabetes · Protocol
- BSurrogate biomarkerHbA1c, fasting glucose and LDL cholesterol in type 2 diabetes and dyslipidemia · Supplement
- B
- BSurrogate biomarkerBlood pressure in adults with obstructive sleep apnea · Device or therapy
- BSurrogate biomarkerSystolic and diastolic blood pressure (DASH, DASH-Sodium) · Protocol
- B
- BSurrogate biomarkerBlood pressure against an unrestricted diet, adults without diabetes · Protocol
- B
- BSurrogate biomarkerBlood pressure reduction (validated surrogate) · Device or therapy
- BSurrogate biomarkerSkin hydration, elasticity and wrinkle depth in adults · Supplement
- BSurrogate biomarkerApnea-hypopnea index and Epworth sleepiness in implanted adults with moderate to severe sleep apnea who cannot use CPAP · Device or therapy
- BSurrogate biomarkerInfluenza in adults aged 60 and older, standard-dose vaccine against placebo · Protocol
- B
- BSurrogate biomarkerResting systolic blood pressure, high-resistance inspiratory muscle strength training · Device or therapy
- BSurrogate biomarkerBody clock timing (melatonin onset) moved earlier, healthy adults · Protocol
- B
- B
- BSurrogate biomarkerApnea severity, daytime sleepiness and blood pressure against inactive control and against CPAP · Device or therapy
- B
- B
- BSurrogate biomarkerNot smoking at 6 months or longer, cytisine · Protocol
- BSurrogate biomarkerNot smoking at 6 months or longer, nicotine e-cigarettes against nicotine replacement · Protocol
- BSurrogate biomarkerNot smoking at 6 months or longer, nicotine replacement · Protocol
- BSurrogate biomarkerNot smoking at 6 months or longer, varenicline · Protocol
- B
- B
- BSurrogate biomarkerApnea-hypopnea index in adults with obesity and moderate to severe obstructive sleep apnea · Longevity drug
- B
- B
- BSurrogate biomarkerLDL and total cholesterol when linoleic-acid oils replace saturated fat · Protocol
- BSurrogate biomarkerSystolic and diastolic blood pressure (Cochrane meta-analysis A study that pools the numbers from several trials into one combined estimate.) · Protocol
- BSurrogate biomarkerPrecancerous skin spots (actinic or solar keratoses), daily sunscreen · Protocol
- BSurrogate biomarkerHbA1c, scaling and root planing in people with diabetes and periodontitis · Protocol
- BSurrogate biomarkerPlaque and gum inflammation, powered against manual toothbrush · Protocol
- BSurrogate biomarkerApnea-hypopnea index in adults with obesity and moderate to severe obstructive sleep apnea · Longevity drug
- B
- BSurrogate biomarkerLDL cholesterol compared with a typical omnivorous diet · Protocol
- CSurrogate biomarkerStructural brain change; cognition unestablished · Device or therapy
- CSurrogate biomarkerWeight regain after diet-induced weight loss, adults with overweight or obesity · Supplement
- CSurrogate biomarkerGlucose and insulin resistance in type 2 diabetes · Protocol
- CSurrogate biomarkerGlycemic control (fasting glucose, HbA1c) · Supplement
- CSurrogate biomarkerSystemic inflammation (CRP) and endothelial function · Supplement
- C
- C
- C
- C
- C
- C
- C
- C
- C
- CSurrogate biomarkerMetabolic markers and pace of aging in healthy non-obese adults · Protocol
- C
- C
- CSurrogate biomarkerHeart rate variability in the hour after immersion · Device or therapy
- C
- CSurrogate biomarkerSystemic inflammatory markers (hs-CRP High-sensitivity C-reactive protein, a blood marker of low-grade inflammation., IL-6) · Supplement
- CSurrogate biomarkerHormone-metabolism / tissue biomarkers A measurable sign in the body, such as a blood test value, used to track a condition or the effect of a treatment. · Supplement
- CSurrogate biomarkerBlood lipoproteins with a larger weekly exercise amount, in overweight adults with mild dyslipidemia · Protocol
- CSurrogate biomarkerBody weight and fat mass with a larger weekly exercise amount, without dieting · Protocol
- CSurrogate biomarkerBlood glucose after a meal or glucose drink · Supplement
- CSurrogate biomarkerCardiac output and filling pressures in heart failure · Supplement
- CSurrogate biomarkerFacial skin quality (topical, after microneedling or RF) · Device or therapy
- CSurrogate biomarkerGlycemic management in type 2 diabetes on metformin or diet alone · Protocol
- CSurrogate biomarkerHbA1c and IGF-1 against an unrestricted diet, adults without diabetes · Protocol
- CSurrogate biomarkerInsulin sensitivity and metabolic markers in metabolic syndrome and obesity · Protocol
- CSurrogate biomarkerGlycated serum protein, inflammatory markers and vaccine antibody response · Supplement
- CSleep quality, mood and heart-rate variability (self-report and surrogate) · Supplement
- CSurrogate biomarkerGlutathione-status and oxidative-stress markers (mixed small trials) · Supplement
- CSurrogate biomarkerGlutathione, oxidative stress and aging markers in older adults (originating group's trial) · Supplement
- CSurrogate biomarkerGlycemic markers in impaired glucose tolerance, metabolic syndrome and type 2 diabetes · Supplement
- C
- CSurrogate biomarkerTelomere length, senescent T cells and cognitive measures in healthy older adults · Protocol
- CSurrogate biomarker2.0 ATA or higher, 100% oxygen by mask or hood · Device or therapy
- CSurrogate biomarkerBlood pressure in implanted adults with obstructive sleep apnea · Device or therapy
- C
- CSurrogate biomarkerWeight and cardiometabolic markers, compared with daily calorie restriction · Protocol
- CSurrogate biomarkerResting systolic blood pressure (surrogate, objective) · Device or therapy
- CSurrogate biomarkerLongevity and cardiometabolic markers in adults · Protocol
- C
- C
- CSurrogate biomarkerBrachial artery flow-mediated dilation in older adults · Supplement
- CSurrogate biomarkerBrain swelling after glioma surgery · Device or therapy
- CSurrogate biomarkerLiver fat in nonalcoholic fatty liver disease · Device or therapy
- CSurrogate biomarkerTotal and LDL cholesterol in adults with overweight, obesity or metabolic disorders · Device or therapy
- CSurrogate biomarkerDNA methylation age, an epigenetic clock A test that estimates biological age from chemical marks on DNA (DNA methylation). · Protocol
- CSurrogate biomarkerApnea-hypopnea index and Epworth sleepiness in obstructive sleep apnea · Device or therapy
- CSurrogate biomarkerBlood NAD+ Nicotinamide adenine dinucleotide, a molecule cells use in energy metabolism. Its level falls with age in some tissues. concentration in healthy middle-aged adults · Supplement
- CSurrogate biomarkerMuscle insulin sensitivity in prediabetic postmenopausal women · Supplement
- C
- CSurrogate biomarkerBlood NAD+ concentration in healthy and clinical adults · Supplement
- CSurrogate biomarkerDNA methylation clocks of biological aging in adults 70 and older · Supplement
- CSurrogate biomarkerLDL cholesterol and liver enzymes (surrogate) · Supplement
- CSurrogate biomarkerApnea-hypopnea index and daytime sleepiness in position-dependent obstructive sleep apnea · Device or therapy
- C
- C
- C
- CSurrogate biomarkerSkin aging (wrinkles, complexion) · Protocol
- C
- CSurrogate biomarkerInsulin sensitivity and glucose control · Device or therapy
- CSurrogate biomarkerImmune cell measures as an adjunct to cancer treatment · Supplement
- C
- C
- CSurrogate biomarkerGrowth hormone and IGF-1 response in older adults · Supplement
- CSurrogate biomarkerSwelling after oral or sinus surgery · Supplement
- CSurrogate biomarkerBlood pressure, insulin sensitivity and glucose after behavioral sleep extension in habitual short sleepers · Device or therapy
- CSurrogate biomarkerEnergy intake and body weight after sleep extension in adults with overweight who sleep under 6.5 hours · Device or therapy
- C
- CSurrogate biomarkerExercise recovery, muscle damage markers and performance · Supplement
- CSurrogate biomarkerGlucose control and insulin resistance in type 2 diabetes · Supplement
- CSurrogate biomarkerHelicobacter pylori colonization markers · Supplement
- CSurrogate biomarkerLiver enzymes in fatty liver or high-normal liver tests · Supplement
- CSurrogate biomarkerNasal response to live attenuated influenza virus · Supplement
- CSurrogate biomarkerTissue markers of cancer risk in biopsy and presurgical trials (lung, breast, prostate) · Supplement
- CSurrogate biomarkerUrinary excretion of airborne pollutants (benzene, acrolein, crotonaldehyde conjugates) · Supplement
- CSurrogate biomarkerNew moles (nevi) in children, sunscreen or sun-protective clothing · Protocol
- C
- C
- CSurrogate biomarkerBlood pressure and artery function, intensive periodontal treatment · Protocol
- CSurrogate biomarkerGum inflammation, flossing and interdental cleaning added to toothbrushing · Protocol
- CSurrogate biomarkerEpigenetic clocks and circulating biomarkers of aging · Device or therapy
- CSurrogate biomarkerWeight and metabolic markers with calories held equal · Protocol
- CSurrogate biomarkerPlasma homocysteine An amino acid in the blood that rises when vitamin B12, folate or B6 are low. · Supplement
- CSurrogate biomarkerTotal testosterone in men with low testosterone · Supplement
- CSurrogate biomarkerBlood pressure and fitness when sauna follows regular exercise · Device or therapy
- C
- C
- CSurrogate biomarkerBone loss in postmenopausal women, measured for the MK-7 component alone · Protocol
- CSurrogate biomarkerArterial stiffness and coronary artery calcification · Supplement
- CSurrogate biomarkerFat mass by DXA (primary) and maximal aerobic capacity, VO2max (secondary), under one weekly session against control · Protocol
- CSurrogate biomarkerBone mineral density (surrogate, objective) · Device or therapy
Graded D, kept apart
Not yet tested in a human trial, or tested and found to do nothing or harm, on the outcome named. Listed in the same order of outcome. 160 in all.
- DHard clinical endpoint · Tested, harm foundAtrial fibrillation recurrence after catheter ablation · Supplement
- DHard clinical endpoint · Not yet testedDementia, heart disease and death after learning the APOE result · Protocol
- DHard clinical endpoint · Tested, harm foundDisability-free survival in healthy adults aged 70 and over · Protocol
- D
- DHard clinical endpoint · Not yet testedLongevity / mortality · Device or therapy
- D
- DHard clinical endpoint · Tested, no benefitHeart attack, stroke and cardiovascular death in adults with moderate to severe obstructive sleep apnea, mostly without daytime sleepiness · Device or therapy
- DHard clinical endpoint · Not yet testedLongevity, healthspan or mortality, taken by mouth · Supplement
- DHard clinical endpoint · Tested, no benefitPressure ulcer prevention, massaged into the skin · Supplement
- DHard clinical endpoint · Tested, no benefitDeath from any cause, five years of supervised exercise on top of guideline-level activity, adults aged 70 to 77 · Protocol
- DHard clinical endpoint · Not yet testedSystemic or intravenous administration for longevity, healthspan or anti-aging · Device or therapy
- DHard clinical endpoint · Not yet testedAging, frailty and longevity in older or healthy adults · Protocol
- D
- DHard clinical endpoint · Tested, no benefitMajor cardiovascular events in people with vascular disease (folic acid with vitamins B6 and B12) · Supplement
- DHard clinical endpoint · Tested, no benefitAll-cause, cardiovascular and cancer mortality in adults unselected for disease · Protocol
- DHard clinical endpoint · Tested, no benefitDementia prevention in older adults · Supplement
- DHard clinical endpoint · Tested, harm foundChronic disease in healthy postmenopausal women, including breast cancer, stroke and blood clots · Protocol
- DHard clinical endpoint · Tested, no benefitDeath from any cause, standard-dose vaccine against placebo, adults aged 60 and older · Protocol
- DHard clinical endpoint · Tested, no benefitHospitalization for influenza or pneumonia, high-dose against standard-dose vaccine, adults aged 65 and older · Protocol
- DHard clinical endpoint · Tested, no benefitPrevention of respiratory infection in adults · Supplement
- DHard clinical endpoint · Tested, no benefitHeart attack, stroke and cardiovascular death, lowering triglycerides with a fibrate added to a statin · Protocol
- DHard clinical endpoint · Tested, harm foundHeart attack, stroke and death, raising HDL cholesterol with CETP inhibitors, niacin or apolipoprotein A1 infusion · Protocol
- DHard clinical endpoint · Not yet testedCardiovascular events and all-cause mortality · Supplement
- DHard clinical endpoint · Tested, no benefitBreast cancer deaths, women aged 39 to 49 · Device or therapy
- DHard clinical endpoint · Tested, no benefitDeath from any cause, women invited to mammography screening · Device or therapy
- DHard clinical endpoint · Tested, no benefitGood neurological outcome after out-of-hospital cardiac arrest · Device or therapy
- DHard clinical endpoint · Tested, no benefitClinical worsening in outpatients with mild to moderate COVID-19 · Device or therapy
- D
- D
- DHard clinical endpoint · Not yet testedLongevity, healthspan or mortality · Supplement
- DHard clinical endpoint · Tested, no benefitPrimary prevention in general-risk adults (mixed EPA+DHA) · Supplement
- D
- DHard clinical endpoint · Tested, no benefitPneumonia from any cause and death, 23-valent polysaccharide vaccine, adults in high-income countries · Protocol
- DHard clinical endpoint · Tested, no benefitPneumonia from any cause, 13-valent conjugate vaccine, adults aged 65 and older · Protocol
- D
- DHard clinical endpoint · Tested, no benefitDeath from any cause, men invited to PSA screening · Device or therapy
- DHard clinical endpoint · Not yet testedDeath, dementia and heart disease · Protocol
- DHard clinical endpoint · Not yet testedSenolytic A compound intended to clear senescent cells: older cells that have stopped dividing but remain in tissue. use for aging outcomes, quercetin alone · Supplement
- DHard clinical endpoint · Tested, no benefitAll-cause death; death, nonfatal heart attack or stroke · Protocol
- DHard clinical endpoint · Tested, no benefitAll-cause mortality when linoleic-acid oils replace saturated fat · Protocol
- DHard clinical endpoint · Tested, no benefitLong-term supplementation in already-replete adults · Supplement
- DHard clinical endpoint · Not yet testedMortality, frailty and longevity · Supplement
- DHard clinical endpoint · Not yet testedSystemic inflammation, cardiovascular or longevity use · Supplement
- DHard clinical endpoint · Not yet testedDementia in older adults · Protocol
- DHard clinical endpoint · Tested, no benefitColorectal cancer deaths and death from any cause, an invitation to screening colonoscopy, adults aged 55 to 64 · Device or therapy
- D
- DHard clinical endpoint · Tested, no benefitDisability-free survival (living without dementia or persistent physical disability) in adults aged 70 and over without cardiovascular disease · Longevity drug
- DHard clinical endpoint · Not yet testedColorectal cancer mortality, fecal immunochemical test (FIT) specifically · Device or therapy
- DHard clinical endpoint · Tested, no benefitHelicobacter pylori eradication, added to standard triple therapy · Supplement
- DHard clinical endpoint · Tested, no benefitBasal cell carcinoma, daily sunscreen · Protocol
- DHard clinical endpoint · Not yet testedBehavioral sun-protection counseling, skin cancer incidence · Protocol
- DHard clinical endpoint · Tested, no benefitOral nicotinamide, skin cancer in organ transplant recipients · Protocol
- D
- DHard clinical endpoint · Tested, no benefitHeart attack, stroke and death, periodontal treatment · Protocol
- DHard clinical endpoint · Tested, no benefitPreterm birth, periodontal treatment during pregnancy · Protocol
- D
- DHard clinical endpoint · Tested, harm foundIntravenous high-dose vitamin C in sepsis · Supplement
- DHard clinical endpoint · Tested, harm foundIntravenous high-dose vitamin C in severe burns · Supplement
- DHard clinical endpoint · Tested, no benefitMajor cardiovascular events · Supplement
- DHard clinical endpoint · Tested, no benefitAll-cause mortality (older adults not selected for vitamin D status) · Supplement
- DHard clinical endpoint · Tested, no benefitCancer prevention (already-replete adults) · Supplement
- DHard clinical endpoint · Tested, no benefitCardiovascular prevention (already-replete adults) · Supplement
- DHard clinical endpoint · Tested, no benefitDeficiency correction & fracture risk (deficient or older adults) · Supplement
- DHard clinical endpoint · Tested, no benefitFracture prevention (already-replete adults) · Supplement
- DHard clinical endpoint · Tested, no benefitMajor cardiovascular events · Supplement
- DHard clinical endpoint · Not yet testedCancer mortality or all-cause mortality in asymptomatic screened adults · Device or therapy
- DHard clinical endpoint · Not yet testedHeart attack, stroke, mortality and longevity · Protocol
- DMeasured function · Tested, harm foundDrugs and supplements chosen because a person carries e4 · Protocol
- D
- DMeasured function · Tested, harm foundStrength and muscle gains when used after resistance training sessions · Device or therapy
- DMeasured function · Tested, no benefitEndurance exercise performance · Supplement
- DMeasured function · Tested, no benefitExercise capacity in heart failure with preserved ejection fraction · Supplement
- DMeasured function · Not yet testedHair growth, human stem-cell-derived exosomes (the products sold) · Device or therapy
- DMeasured function · Tested, no benefitCognition in people with Alzheimer's disease and hearing loss · Protocol
- DMeasured function · Tested, no benefitCognitive decline over 3 years in adults aged 70 to 84 with untreated hearing loss, overall · Protocol
- DMeasured function · Tested, no benefitStrength and hypertrophy in resistance-trained young men · Supplement
- DMeasured function · Tested, no benefitAerobic and endurance exercise performance, free L-citrulline · Supplement
- DMeasured function · Not yet testedOlfactory recovery after COVID-19, luteolin alone · Supplement
- DMeasured function · Tested, harm foundMuscle and mitochondrial gains from exercise training in healthy older adults · Longevity drug
- DMeasured function · Not yet testedDaily low-dose methylene blue for memory or cognition · Supplement
- DMeasured function · Tested, no benefitEndurance exercise performance and training adaptation · Supplement
- DMeasured function · Tested, no benefitPhysical function in healthy older adults · Supplement
- DMeasured function · Not yet testedHealthy adults: outdoor light within a fixed window after waking, for sleep, mood or energy · Protocol
- DMeasured function · Tested, harm foundOlder adults with memory impairment living at home: 30 minutes of bright light within 30 minutes of rising · Protocol
- DMeasured function · Tested, no benefitCognition in mild cognitive impairment · Supplement
- DMeasured function · Tested, harm foundEarly Parkinson disease · Supplement
- DMeasured function · Tested, no benefitCognitive function in older adults · Protocol
- DMeasured function · Tested, no benefitMemory and cognition in older adults, soy-derived phosphatidylserine (the form sold) · Supplement
- DMeasured function · Tested, no benefitMemory in older adults with memory complaints · Protocol
- DMeasured function · Tested, no benefitExercise recovery, objective function (jump, MVC) · Device or therapy
- DMeasured function · Tested, no benefitVisceral adiposity and physical function (chair-stand repetitions) in older adults · Longevity drug
- DMeasured function · Tested, no benefitCognition, falls, quality of life and mortality · Protocol
- DMeasured function · Tested, harm foundExercise training adaptations in older men (resveratrol added to training) · Supplement
- DMeasured function · Tested, no benefitMemory in older adults with subjective cognitive decline · Supplement
- DMeasured function · Tested, no benefitPreventing dementia and cognitive decline in older people · Longevity drug
- DMeasured function · Tested, no benefitCognition in schizophrenia · Supplement
- DMeasured function · Tested, no benefitOutcome after subarachnoid hemorrhage (SFX-01, a stabilized sulforaphane drug) · Supplement
- DMeasured function · Tested, no benefitCognitive test scores, cataract surgery in cognitively normal older adults · Protocol
- DMeasured function · Tested, no benefitEyesight, community vision screening of people aged 65 and older · Protocol
- DSelf-report · Tested, no benefitFatigue in quiescent inflammatory bowel disease · Supplement
- DSelf-report · Tested, no benefitHealth behavior and risk factors after learning the APOE result · Protocol
- DSelf-report · Tested, no benefitOsteoarthritis pain and inflammation markers, bromelain alone · Supplement
- D
- DTested, no benefitADHD symptoms in children and adolescents (self-report, blinding-sensitive) · Device or therapy
- DSelf-report · Tested, no benefitMigraine prevention · Supplement
- DSelf-report · Tested, no benefitOrthopedic / knee osteoarthritis / cartilage · Device or therapy
- DSelf-report · Tested, no benefitDiet quality and health measures with advice tailored to genotype, compared with personalized advice that does not use genotype · Device or therapy
- D
- DSelf-report · Tested, no benefitSymptom severity in Gulf War illness, luteolin alone · Supplement
- DBlinded clinician rating · Tested, no benefitPrevention of delirium in the general intensive care unit · Supplement
- DBlinded clinician rating · Tested, no benefitMotor symptoms in Parkinson's disease · Device or therapy
- DBlinded clinician rating · Tested, no benefitSpasm control in infants with epileptic spasms, added to standard treatment · Device or therapy
- DSelf-report · Tested, no benefitKnee osteoarthritis symptoms · Supplement
- DSelf-report · Tested, no benefitKnee or hip osteoarthritis, pain and function · Supplement
- DBlinded clinician rating · Tested, no benefitMajor depressive disorder, SAM-e added to an antidepressant · Supplement
- DSelf-report · Tested, no benefitChronic or recurrent sinus symptoms · Device or therapy
- DSelf-report · Tested, no benefitCommon cold symptoms · Device or therapy
- DBlinded clinician rating · Tested, no benefitClinical status in hospitalized community-acquired pneumonia (SFX-01) · Supplement
- DSelf-report · Tested, no benefitCommon cold symptoms, breathing hot sauna air during a cold · Device or therapy
- DSelf-report · Tested, no benefitFalls, expedited second-eye cataract surgery in women over 70 · Protocol
- DSelf-report · Tested, harm foundFalls, eye examination with treatment of vision problems in frail older people · Protocol
- DSelf-report · Tested, no benefitFalls, single-lens distance glasses for older multifocal wearers · Protocol
- DSelf-report · Tested, no benefitPreventing colds in the general population · Supplement
- DSelf-report · Tested, no benefitShortening a cold by starting vitamin C after symptoms begin · Supplement
- DSelf-report · Tested, no benefitPrevention of depression in adults aged 50 and over · Supplement
- DSurrogate biomarker · Tested, no benefitInsulin sensitivity and metabolic markers in overweight or insulin-resistant adults · Supplement
- D
- D
- D
- D
- DSurrogate biomarker · Tested, no benefitMusculoskeletal measures (strength, lean mass, bone) in prediabetes or type 2 diabetes · Supplement
- DSurrogate biomarker · Tested, no benefitLowering inflammation · Device or therapy
- DSurrogate biomarker · Tested, no benefitBone mineral density in postmenopausal women · Supplement
- DSurrogate biomarker · Tested, no benefitFinger ulcers in systemic sclerosis, applied to the skin · Supplement
- DSurrogate biomarker · Tested, no benefitBlood pressure · Supplement
- DSurrogate biomarker · Tested, no benefitGlutathione redox status in healthy older adults · Supplement
- DSurrogate biomarker · Tested, no benefit1.3 to 1.5 ATA, concentrator air · Device or therapy
- DSurrogate biomarker · Tested, no benefitAcute glycemic control, T2DM · Device or therapy
- DSurrogate biomarker · Tested, no benefitSleep apnea severity (apnea-hypopnea index) · Device or therapy
- D
- DSurrogate biomarker · Not yet testedBlood pressure · Protocol
- DSurrogate biomarker · Tested, no benefitIncidence of late-stage (III and IV) cancer at diagnosis, a stage-shift surrogate for cancer mortality · Device or therapy
- DSurrogate biomarker · Tested, no benefitInsulin sensitivity in obese insulin-resistant men · Supplement
- DSurrogate biomarker · Tested, no benefitCollagen turnover and cardiac remodeling markers in hypertension with raised galectin-3 · Supplement
- DSurrogate biomarker · Not yet testedPSA kinetics in non-metastatic biochemically relapsed prostate cancer · Supplement
- DSurrogate biomarker · Tested, harm foundLDL cholesterol in adults enrolled for raised cholesterol · Supplement
- D
- DSurrogate biomarker · Tested, no benefitGlycemic control in metabolic syndrome and related disorders · Supplement
- DSurrogate biomarker · Tested, no benefitBlood glucose, lipids and blood pressure in type 2 diabetes and metabolic syndrome · Supplement
- DSurrogate biomarker · Not yet testedBody composition and lean mass in older adults · Supplement
- DSurrogate biomarker · Not yet testedAny health outcome of regular steam room use, steam compared with no steam · Device or therapy
- DSurrogate biomarker · Tested, no benefitAirway inflammation and lung function (asthma, COPD, ozone exposure) · Supplement
- DSurrogate biomarker · Tested, no benefitBlood pressure and endothelial function in hypertension · Supplement
- DSurrogate biomarker · Tested, no benefitNRF2 target gene expression (the proposed mechanism) · Supplement
- DSurrogate biomarker · Tested, no benefitPSA after radical prostatectomy for prostate cancer (biochemical recurrence) · Supplement
- DSurrogate biomarker · Tested, no benefitHeart rate variability when sauna follows regular exercise · Device or therapy
- DSurrogate biomarker · Tested, no benefitVascular function in stable coronary artery disease · Device or therapy
- DSurrogate biomarker · Tested, no benefitHeart rate variability in healthy adults · Device or therapy
- D
- D