Turmeric vs. placebo: will this spice soothe your aching thumb?
NCT ID NCT06359665
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether turmeric (curcumin) can reduce pain and improve function in people with thumb-joint arthritis. One hundred adults will take turmeric capsules for four weeks and a placebo for another four weeks, then compare results. The goal is to see if this common spice offers real relief for a common, painful condition.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- curcumin (turmeric)
- What this could lead to
- If it works, this could point toward a natural, over-the-counter option for managing thumb arthritis pain.
- What could go wrong
- This is a very early phase 1 trial with only 100 people. Turmeric may work no better than a placebo, and results may not apply to everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2025
- Expected to finish
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Feb 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Provision of signed and dated informed consent form. 2. Stated willingness to comply with all study procedures and availability for the duration of the study. 3. Male or female, aged 18 years or older. 4. For females, must be willing to use an approved form of birth control during this study. Acceptable forms of birth control: * Norplant * IUD (intrauterine device) * Birth Control Patch * Depo-Provera * Sterilization The following may be used if combined with other birth control methods: * Condoms * Diaphragm * Jellies or foam * Cervical cap * Sponge 5. For males, must be willing to not father a baby for the duration of the study and for 90 days after the last dose of study drug, or donate to a sperm back during this time. Must be willing to use an approved form of birth control during this time. Acceptable forms of birth control: * Condoms * Sterilization 6. Daily visual analog pain greater than 5 and ≤ 9 out of 10. 7. Duration of pain for greater than 30 days. 8. Presence of radiographically confirmed diagnosis of thumb basal joint arthritis Exclusion Criteria: 1. Participant does not speak English. 2. Participant is blind. 3. Severe cardiac, pulmonary, liver, gastrointestinal and hematological disease (including coagulopathy), and /or renal disease. 4. Abnormal hematological, coagulation, and/or liver function test results. 5. Coumadin use at time of screening. 6. Use of any anticoagulant and antiplatelet medication. 7. History of mental illness. 8. Participant who is incarcerated. 9. History of drug or substance abuse. 10. Pre-existing curcumin or turmeric product usage within 3 months of the study period. 11. Participant has had a corticosteroid injection ≤ 60 days prior. 12. Participant has had prior surgery for osteoarthritis treatment 13. Participant who has fibromyalgia and post-operative pain. 14. Females who are pregnant, nursing or planning a pregnancy 15. Participants within 14 days of the study procedure taking prescription or non-prescription medication which are substrates of CYP3A4: * Itraconazole, * Ketoconazole, * Azamulin, * Troleandomycin, * Verapamil, * John's wart, * Phenobarbital, 16. Participants within 14 days of the study procedure taking prescription or non-prescription medication which are substrates of CYP2C19: * Nootkatone, * Ticlopidine, * Rifampin, * Omeprazole), 17. Participants within 14 days of the study procedure taking prescription or non-prescription medication which are substrates of CYP2C8: * Montelukast, * Quercetin, * Phenelzine, * Rifampin, * Clopidogrel , 18. Participants within 14 days of the study procedure taking prescription or non-prescription medication which are substrates of CYP2C9: * Sulfaphenazole, * Tienilic acid, * Carbamazepine, * Apoflutamide , * Fluconazole, * Celecoxib, 19. Participants within 14 days of the study procedure taking prescription or non-prescription medication which are substrates of CYP1A2: * alpha-Naphthoflavone, * Furafylline, * Phenytoin, * Rifampin, * Ritonavir, * smoking, * Teriflunomide, * Ciprofloxacin, * oral contraceptives, * Allopurinol 20. Participants within 14 days of the study procedure taking prescription or non-prescription medication which are substrates of CYP2B6 : * Sertraline, * Phencyclidine, * Thiotepa, * Ticlopidine, * Carbamazepine, * Efavirenz, * Rifampin, * Bupropion)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Virginia
Charlottesville, Virginia, 22903, United States