Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07089381

Efficacy and Safety of Resveratrol in Patients With Rheumatoid Arthritis

Led by Ain Shams University · Updated on 2025-07-28

118

Participants Needed

1

Research Sites

17 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Brief Title

Efficacy and Safety of Resveratrol in Patients With Rheumatoid Arthritis.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients over 18 years old
  • Established diagnosis of rheumatoid arthritis according to ACR/EULAR 2010 criteria
  • Moderate to high disease activity with DAS28-CRP score greater than 3.2
  • Receiving stable regimen of conventional synthetic DMARDs for at least the past 3 months
Not Eligible

You will not qualify if you...

  • Receiving biologic DMARDs therapy for rheumatoid arthritis
  • Taking any other anti-inflammatory drugs
  • Taking any other antioxidants
  • Pregnant or lactating women
  • Other rheumatological, inflammatory diseases or malignancies
  • Smokers
  • Thyroid illnesses
  • Impaired liver function with transaminases three times above normal limits
  • Impaired kidney function with eGFR less than 30 ml/min

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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

Follow-up

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

Trial Site Locations

Total: 1 location

1

Department of Rheumatology at Ain Shams university hospital, Cairo, Egypt

Cairo, Egypt

Actively Recruiting

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Research Team

R

Rana El-Dash, MsC

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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Published Research Related To This Trial

Effect of Resveratrol on Markers of Oxidative Stress and Sirtuin 1 in Elderly Adults with Type 2 Diabetes.

Beatriz Isabel García-Martínez, Mirna Ruiz-Ramos, José Pedraza-Chaverri...

https://pubmed.ncbi.nlm.nih.gov/37108584