Therapeutic Potential of Plant-Derived Compounds and Plant Extracts in Rheumatoid Arthritis-Comprehensive Review.
Mateusz Kciuk, Anjali Garg, Manni Rohilla...
https://pubmed.ncbi.nlm.nih.gov/39061843/Actively Recruiting
Led by Ain Shams University · Updated on 2025-07-28
118
Participants Needed
1
Research Sites
17 weeks
Total Duration
Researchers are evaluating the effects of resveratrol in adults with moderate to high active rheumatoid arthritis RA. The study aims to understand how resveratrol impacts inflammation, oxidative stress, disease activity, and quality of life in patients already receiving standard RA treatment. The trial is sponsored by Ain Shams University and involves 118 eligible patients randomly assigned to two groups. One group will receive standard RA treatment plus a daily 1 gram dose of resveratrol for three months, while the other group will receive only the standard treatment for the same period. Resveratrol is given as a single 1000 mg tablet once daily. Patients are monitored for 3 months during treatment. Participants will undergo assessments of inflammation and oxidative stress by measuring serum markers such as Sirtuin 1 SIRT1, Myeloperoxidase MPO, and C-reactive protein CRP. Disease activity will be evaluated using the DAS28 score, and quality of life will be measured using the Health Assessment Questionnaire Disability Index HAQ-DI. Researchers will also monitor for any adverse effects related to resveratrol throughout the study period, which lasts from 3 to 6 months.
CONDITIONS
Efficacy and Safety of Resveratrol in Patients With Rheumatoid Arthritis.
R
Rana El-Dash, MsC
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Ain Shams University
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 3 months
Participants receive standard treatment for rheumatoid arthritis, with some receiving Resveratrol 1 gm daily in addition to standard treatment, for 3 months.
Regular visits during treatment period as per usual care
Duration - 3 months
Participants are monitored to investigate effects on inflammation, disease activity, and quality of life after treatment ends.
Visits from 3 to 6 months after treatment begins
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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https://pubmed.ncbi.nlm.nih.gov/29194364/Ain Shams University
Lead Sponsor