Resveratrol ameliorates rheumatoid arthritis via activation of SIRT1-Nrf2 signaling pathway.
Gaoyuan Wang, Xinxin Xie, Lingli Yuan...
https://pubmed.ncbi.nlm.nih.gov/31883358Actively 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.
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
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
Total: 1 location
1
Department of Rheumatology at Ain Shams university hospital, Cairo, Egypt
Cairo, Egypt
Actively Recruiting
R
Rana El-Dash, MsC
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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