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The effect of combinant antioxidant supplementation on blood in patient with rheumatoid arthritist

The effect of combinant antioxidant supplementation on blood ADMA and VEGF levels and clinical outcomes in patient with rheumatoid arthritist

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201203116934N2
Enrollment
40
Registered
2012-05-30
Start date
2012-06-20
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

Rhumatoid arthritis. Seropositive rheumatoid arthritis

Interventions

A tablet supplementation antioxidant compounds, including supplementation with a combination of selenium, zinc, vitamin A, E and C to form oral supplement "Celine Plus" is the order of 50 mg, 8 mg, 40
Treatment - Drugs

Sponsors

Pharmaceutical research center, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: People with diagnosis of Rheumatoid arthritis disease according to American College of Rheumatology criteria (ACR) is confirmed. The doctor diagnosed according to criteria ACR (at least 4 criteria for six weeks : 1 - morning stiffness in the joint for at least an hour or more 2 - articular arthritis in three areas or more4: hand joint arthritis 5- symmetrical arthritis 5 - rheumatoid nodules 6 - positive rheumatoid factor 7 - typical radiographic changes in the wrist and hand) in adult patients with rheumatoid arthritis and patients visiting the doctor, at least for the past two months have not had a treatment change. Selected at random from among eligible women 30 -60 years old admitted with mild to moderate range of severity of illness would be a specialist; if DAS (Disease Activity Score) below 3/2 is a mild disease and the DAS (Disease Activity Score) is between 3/2-5/1, moderate severity is defined .

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Determine and compare the clinical improvement in patients with rheumatoid arthritis before and after intervention. Timepoint: Before and 3 month after intervention. Method of measurement: DAS questionnaire.;ADMA concentrations in the serum of patients with rheumatoid arthritis before and three months after the administration of antioxidants. Timepoint: Previous intervention three months after the intervention began. Method of measurement: ELISA method.;Determine changes in serum VEGF rheumatoid arthritis before and three months after the administration of antioxidants. Timepoint: Before and 3 month after intervention. Method of measurement: ELISA.

Secondary

MeasureTime frame
Investigate the effects of antioxidant drugs. Timepoint: Before and three months after intervention. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSousan Kolai

Tabriz University of Medical Sciences

susan.kolahi@gmail.com+98 41 1337 1217

Outcome results

None listed

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