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C

Listed compound, not counted as a supplement

DMSO (Dimethyl Sulfoxide)

Knee osteoarthritis pain, gel applied to the skin.

Grade C: human trials exist, but they are small, mixed or not yet repeated. This is not a finding that it does not work. How to read a grade →

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In plain words

DMSO is a liquid solvent sold as a gel for joint pain, and lately taken by mouth for long life. Rubbed on the skin, it eased knee arthritis pain in one German study. A larger study of 775 people found it no better than a dummy treatment. Studies of shoulder and elbow pain were small. No study has tested DMSO by mouth for aging or long life.

The C belongs to one of the six uses graded on this record. The other five carry their own letters.

Grades by use · each use graded on its own evidence
CKnee osteoarthritis pain, gel applied to the skinself-report
As studied, and the trials
As studied
DoseApplied to the knee for 3 weeks in the positive trial; a DMSO-containing solution 40 drops four times a day for 12 weeks in the null one
FormDMSO 25% gel
PopulationAdults with symptomatic knee osteoarthritis, 112 in the positive trial and 775 across five arms in the null one
Duration3 to 12 weeks

The positive trial is the smaller and shorter one. In the larger trial, DMSO was the vehicle for a diclofenac solution and was also given alone as a control arm; alone, it did not beat placebo An inactive substitute made to look like the real treatment, so participants cannot tell which one they received. on pain or function. The systematic review A review that searches for every study on a question using a method set in advance, then assesses them together. found no definitive conclusion could be drawn from the DMSO trials.

CAcute shoulder or elbow tendon pain, gel applied to the skinself-report
As studied, and the trials
As studied
DoseThree times a day
FormDMSO 10% gel
Population157 adults with acute tendon pain at the shoulder or elbow, treated within 72 hours of onset
Duration14 days

One multicenter trial, positive: 44% pain-free at 14 days versus 9% on the gel base. It has not been repeated by another group, and a single unrepeated trial is a C on this site.

CComplex regional pain syndrome type I, cream applied to the skinself-report
As studied, and the trials
As studied
DoseFive times a day
FormDMSO 50% in a fatty cream
Population32 patients with acute reflex sympathetic dystrophy after injury; 146 patients with complex regional pain syndrome type I in the comparison with N-acetylcysteine
Duration2 months to 17 weeks

The placebo-controlled trial was small and positive. The larger trial compared DMSO with oral N-acetylcysteine rather than with placebo and found them about equal. Both trials came from the same Dutch group, and the Cochrane overview rates the evidence low certainty.

DFinger ulcers in systemic sclerosis, applied to the skinTESTED, NO BENEFITsurrogate biomarker A measurable sign in the body, such as a blood test value, used to track a condition or the effect of a treatment.
As studied, and the trials
As studied
DoseApplied topically to the ulcers
FormDMSO 2% and 70%, versus normal saline
Population84 patients with systemic sclerosis and finger ulcers
DurationTreatment course of the multicenter trial

Tested against saline and not better on any measure. The higher concentration added skin toxicity without adding healing.

DPressure ulcer prevention, massaged into the skinTESTED, NO BENEFIThard clinical endpoint An outcome that matters directly to a person and is counted without judgment, such as death, heart attack, stroke or fracture.
As studied, and the trials
As studied
DoseMassage at pressure points, compared with an indifferent cream and with position changes alone
FormDMSO cream used for massage
PopulationNursing home residents prone to pressure ulcers
DurationCrossover A trial design in which each participant receives both the treatment and the comparison, one after the other, and serves as their own control. periods of the trial

Tested in the setting where an earlier pilot had suggested benefit, and the benefit did not appear.

DLongevity, healthspan or mortality, taken by mouthhard clinical endpoint The outcome a trial measures to decide whether the treatment worked, such as heart attacks, blood pressure or a symptom score.
As studied, and the trials
As studied
DoseNot applicable
FormNot applicable
PopulationNo randomized human trial has been run for this endpoint
DurationNot applicable

No human randomized trial has tested DMSO against aging, healthspan or lifespan, by mouth or any other route. The nearest human data are single-author trials of oral DMSO after cancer surgery reporting longer survival in advanced cancer, never repeated in thirty years. They are cited so a reader can find them, and they do not carry a letter.

Read the grade that matches your goal. How EBL grades by use →

C DMSO (dimethyl sulfoxide) structure
C2H6OS
Organosulfur solvent · 2D structure
Dose studied
10% to 50%, applied to the skin
Form graded
Topical gel or cream
C Grade C

A letter describes the human evidence, not the product, the manufacturer, or the ingredient's worth.

See the full evidence record →

DMSO (dimethyl sulfoxide) applied to the skin for knee osteoarthritis pain, graded on human trial evidence. Longevity: Grade D, no human trial.

RCTWhy this flag? ▾

At least one randomized, placebo-controlled human trial, typically double-blinded Neither the participants nor the people assessing them know who received the real treatment until the trial ends..

Learn more about evidence flags →
Not replicatedWhy this flag? ▾

Evidence rests on a single trial that has not been independently replicated The same finding reproduced by a separate research group. A result seen once can be chance or bias; a replicated one is harder to explain away.. Treat as provisional.

Learn more about evidence flags →
Why this gradeGrade C, small or unreplicated trials. The reasoning, and what the grade does not cover.
Why this grade

Grade C, and it rests on the use with the most randomized evidence behind it: DMSO gel applied to the skin for knee osteoarthritis pain. One German trial of a 25% gel in 112 patients found less pain than with the gel base alone (Eberhardt et al., 1995; 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. 8529985). The largest trial run, 775 people with knee osteoarthritis over 12 weeks, included the DMSO solution on its own as one of its five arms and found it no better than placebo on pain or function (Simon et al., 2009; PMID 19380203). A systematic review of the DMSO knee trials concluded that no definitive conclusion can be drawn and flagged possible unblinding (PMID 18417375). A positive trial followed by a larger null one is a replication that failed, which is a C on this site. Pain is reported by the person, which would cap the record at B even if the trials agreed.

WHAT THIS GRADE DOES NOT COVERAging, healthspan and lifespan, where no human randomized trial has been run at all, so that use is a D. DMSO taken by mouth, which is how it is now marketed for longevity. A series of 1990s trials from a single author, A.S. Salim, gave oral DMSO after cancer surgery and reported longer survival (PMID 8493453, PMID 1591948). Nobody has repeated them in thirty years, and they are listed here as context, not as evidence that moves a letter. The bladder instillation for interstitial cystitis is a prescription drug, RIMSO-50, and it carries its own grade on its own record.

A grade describes the human evidence for a named use. It is not advice, and it is not a judgment on any individual prescription. How the letters are decided →

Who responds: this record's trial reading reports no subgroup that identifies who responds.

As studied: dose, form, population and duration for every use
As studied
Knee osteoarthritis pain, gel applied to the skin
FormDMSO 25% gel
DoseApplied to the knee for 3 weeks in the positive trial; a DMSO-containing solution 40 drops four times a day for 12 weeks in the null one
PopulationAdults with symptomatic knee osteoarthritis, 112 in the positive trial and 775 across five arms in the null one
Duration3 to 12 weeks
Acute shoulder or elbow tendon pain, gel applied to the skin
FormDMSO 10% gel
DoseThree times a day
Population157 adults with acute tendon pain at the shoulder or elbow, treated within 72 hours of onset
Duration14 days
Complex regional pain syndrome type I, cream applied to the skin
FormDMSO 50% in a fatty cream
DoseFive times a day
Population32 patients with acute reflex sympathetic dystrophy after injury; 146 patients with complex regional pain syndrome type I in the comparison with N-acetylcysteine
Duration2 months to 17 weeks
Finger ulcers in systemic sclerosis, applied to the skin
FormDMSO 2% and 70%, versus normal saline
DoseApplied topically to the ulcers
Population84 patients with systemic sclerosis and finger ulcers
DurationTreatment course of the multicenter trial
Pressure ulcer prevention, massaged into the skin
FormDMSO cream used for massage
DoseMassage at pressure points, compared with an indifferent cream and with position changes alone
PopulationNursing home residents prone to pressure ulcers
DurationCrossover periods of the trial
Longevity, healthspan or mortality, taken by mouth
FormNot applicable
DoseNot applicable
PopulationNo randomized human trial has been run for this endpoint
DurationNot applicable

A grade describes the intervention that was tested. Where the product on the shelf differs from it, this says so.

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Safety lookup
Evidence last reviewed September 2026
Dose

Applied to the skin in every trial this record grades. Knee osteoarthritis: 25% gel for 3 weeks (PMID 8529985). Acute tendon pain: 10% gel three times a day for 14 days (PMID 8194818). Complex regional pain syndrome: 50% in a fatty cream, five times a day, for 2 months to 17 weeks (PMID 8721469, PMID 12670672). No oral dose has been tested in a randomized trial against any aging outcome, so none can be stated.

Form note

The trials used prepared gels and creams at 10% to 50%. A liquid sold at a higher concentration is not what these trials tested. The 70% solution is the one that caused skin toxicity in the scleroderma trial (PMID 3884019). The prescription bladder product, RIMSO-50, is a 50% solution and is graded on its own record.

Timing in the trials

In the cited trials DMSO was applied to the skin, three to five times a day depending on the trial (PMID 8194818, PMID 12670672). No trial tied it to a time of day.

Checked against the published summaries; the full papers could not be read. What the cited trials did, not a schedule. Every supplement, by trial timing →

Contraindications A condition or medication that makes a treatment unsafe or unsuitable for a particular person. · read before use
Contraindications and cautions

Broken or ulcerated skin at high concentration: in the scleroderma finger-ulcer trial, over a quarter of patients on 70% DMSO were withdrawn for significant skin toxicity (PMID 3884019). Pregnancy and breastfeeding, where it has not been studied. The effect people notice first is a garlic-like taste and breath, with skin odor that the prescription label for the bladder product says can last up to 72 hours. A systematic review of 109 studies found gastrointestinal and skin reactions the most common, mostly transient, and more frequent at higher doses (PMID 31489176).

Drug Interactions

Sulindac: in a randomized crossover study in 8 healthy men, oral DMSO taken an hour before sulindac lowered the drug's active metabolite by about 30% (PMID 6854139). Anything else on the skin: DMSO is used in prescription gels precisely because it carries other substances through the skin, as it does for diclofenac in the knee trials (PMID 15477437). What is on the skin when it is applied goes in with it.

Sources for the above

DMSO lowered the active form of sulindac in a small human study. Sulindac is converted in the body to an active sulfide. In a randomized crossover study in 8 healthy men, oral DMSO taken an hour before sulindac lowered the active metabolite by about 30% on average, with a range of 7% to 56%. The authors suggest DMSO may reduce sulindac's effect. The study measured blood levels, not pain relief. Swanson et al. (Journal of Laboratory and Clinical Medicine, 1983; PMID 6854139): randomized crossover pharmacokinetic study, 8 healthy men, 400 mg sulindac with and without 30 mL of 70% DMSO by mouth.

DMSO carries other substances through the skin. DMSO is used in prescription topical products as an absorption enhancer, the role it plays in the diclofenac solution tested for knee osteoarthritis. The same property means whatever else is on the skin when DMSO is applied is carried in with it. Roth and Shainhouse (Archives of Internal Medicine, 2004; PMID 15477437): topical diclofenac solution containing the absorption enhancer dimethyl sulfoxide, randomized against a vehicle control.

How to track

The trials measured pain on a scale and, in the tendon trial, joint mobility. There is no blood marker that reports whether DMSO is working.

Primary evidence14 papers, each linked to its PubMed record.
Primary evidence

Eberhardt et al. (Fortschritte der Medizin, 1995; PMID 8529985): 112 patients with active knee osteoarthritis, 25% DMSO gel versus gel base for 3 weeks, less pain on loading, at rest and on pressure. Simon et al. (Pain, 2009; PMID 19380203): 775 patients with knee osteoarthritis, five arms over 12 weeks; the DMSO vehicle arm did not differ from placebo. Brien et al. (Osteoarthritis and Cartilage, 2008; PMID 18417375): systematic review of four DMSO trials in 681 patients, no definitive conclusion, poor methodology. Kneer et al. (Fortschritte der Medizin, 1994; PMID 8194818): 157 patients with acute shoulder or elbow tendon pain, 10% gel versus gel base for 14 days, 44% pain-free versus 9%. Zuurmond et al. (Acta Anaesthesiologica Scandinavica, 1996; PMID 8721469): 32 patients with acute reflex sympathetic dystrophy, 50% DMSO cream versus cream base, better disease scores. Perez et al. (Pain, 2003; PMID 12670672): 146 patients with complex regional pain syndrome type I, DMSO cream versus oral N-acetylcysteine, no overall difference. Ferraro et al. (Cochrane Database of Systematic Reviews, 2023; PMID 37306570): low-certainty evidence for DMSO in complex regional pain syndrome. Williams et al. (Arthritis and Rheumatism, 1985; PMID 3884019): 84 patients with systemic sclerosis finger ulcers, 2% and 70% DMSO versus saline, no difference. Duimel-Peeters et al. (International Journal of Nursing Studies, 2007; PMID 17553503): massage with DMSO cream did not prevent pressure ulcers better than position changes alone. Kollerup Madsen et al. (F1000Research, 2018; PMID 31489176): systematic review of adverse reactions across 109 studies. Swanson et al. (Journal of Laboratory and Clinical Medicine, 1983; PMID 6854139): DMSO lowered the active metabolite of sulindac. Roth and Shainhouse (Archives of Internal Medicine, 2004; PMID 15477437): DMSO as the absorption enhancer in a topical diclofenac solution. CONTEXT ONLY, NOT GRADED: Salim (Tumor Biology, 1993; PMID 8493453) and Salim (Chemotherapy, 1992; PMID 1591948), single-author randomized trials of oral DMSO after cancer surgery reporting longer survival, never independently repeated.

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FDA / DSHEA statement

These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. The grade on this page describes the strength of published human trial evidence in the populations studied. It is not a recommendation for any individual and is not medical advice. Starting, stopping or changing any supplement or medication is a decision for your physician.

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