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Effect of pomegranate supplement on Rheumatoid Arthritis patients

The effect of pomegranate extract on clinical index, inflammation markers and oxidative stress of Rheumatoid Arthritis patient in 1390

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201202183236N2
Enrollment
50
Registered
2012-03-07
Start date
2011-11-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Rheumatoid arthritis. Condition 2: Rheumatoid arthritis. Other rheumatoid arthritis Seropositive rheumatoid arthritis

Interventions

Intervention 1: Placebo(2 capsules) intake per day, for 2 months. Intervention 2: Pomegranate supplement(2 capsules) intake is equivalent to 500 mg per day, for 2 months.
Placebo
Treatment - Drugs
Placebo(2 capsules) intake per day, for 2 months
Pomegranate supplement(2 capsules) intake is equivalent to 500 mg per day, for 2 months

Sponsors

Vice chancellor for research OF Shiraz university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Rheumatoid arthritis patients which their disease diagnosed according to the revised American Rheumatism Association criteria, ages between 18-65 years old, RA patients who don’t have enough clinical and laboratory response to conventional disease modifying anti rheumatic drugs (Methotrexate, Hydroxychloroquine, Sulphasalazine, and prednisolone), No drug type and dose fluctuation since 1 month prior to the study and during intervention period. Exclusion criteria: Presence of Chronic disease such as diabetes, cardiovascular, hepatic, kidney, gastrointestinal diseases, and severe infection, smoking, Alcohol consumption, use of supplements (antioxidants, multivitamins,...), patients with known allergy and food intolerance.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Disease activity. Timepoint: Before and 2 months after intervention. Method of measurement: DAS 28.;Disability and Pain scales. Timepoint: Before and 2 months after intervention. Method of measurement: health Assessment Questionnaire for Rheumatoid Arthritis patients.;Duration of morning stiffness. Timepoint: Before and 2 months after intervention. Method of measurement: Taking history and Questionnaire.

Secondary

MeasureTime frame
Glutathione peroxidase. Timepoint: Before and 2 months after intervention. Method of measurement: ELIZA kit.;MDA. Timepoint: Before and 2 months after intervention. Method of measurement: Spectrophotometry.;CRP. Timepoint: Before and 2 months after intervention. Method of measurement: ELIZA kit.;ESR. Timepoint: Before and 2 months after intervention. Method of measurement: Westergren.;MMP3. Timepoint: Before and 2 months after intervention. Method of measurement: ELIZA kit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElham Tavakoli

School of health & nutrition, Shiraz University of Medical Sciences

elham1tavakoli@yahoo.com+98 71172510018

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026