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The effect of sea buckthorn on clinical symptoms of rheumatoid arthritis

A clinical trial of comparing the effect of sea buckthorn extract with placebo on clinical symptoms of patients with rheumatoid arthritis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210630051742N1
Enrollment
30
Registered
2021-11-13
Start date
2021-12-22
Completion date
Unknown
Last updated
2021-11-29

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

Conditions

Rheumatoid arthritis. Rheumatoid arthritis with rheumatoid factor

Interventions

Intervention 1: Intervention group: 500 milligram capsule of sea buckthorn extract, once daily, up to 90 days, manufactured in School of Persian and complementary medicine of Mashhad university of med

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Newly diagnosed patient based on ACR/EULAER criteria for rheumatoid arthritis. Patient who has received no medication for rheumatoid arthritis until now. Disease severity should be between 2.5 to 5.5 based on DAS criteria.

Exclusion criteria

Exclusion criteria: Patient MI history Patient has hyperlipidemia Patient has liver or kidney impaired function. Patient has any neoplasm Patient has psychiatric diseases. There is active infection in patient's body. Patient takes vitamin/mineral supplements. Patient takes medications like thyroid hormones, Anti hypertensives, contraceptives, diuretics and beta-blockers. Patient drinks alcohol or smokes. Patient has any allergy to sea buckthorn. Patient is pregnant or breastfeeds. Disease severity is above 5.5 based on DAS criteria.

Design outcomes

Primary

MeasureTime frame
Severity of pain. Timepoint: before intervention and 30, 45, 90 days after intervention. Method of measurement: visual analog scale.;Number of tender joints. Timepoint: before intervention and 30, 45, 90 days after intervention. Method of measurement: Disease Activity Score Calculator for Rheumatoid Arthritis.;Number of swollen joints. Timepoint: before intervention and 30, 45, 90 days after intervention. Method of measurement: Disease Activity Score Calculator for Rheumatoid Arthritis.;ESR. Timepoint: Before intervention and 90 days after intervention. Method of measurement: Blood test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Roshanak Salari

Mashhad University of Medical Sciences

Salarir@mums.ac.ir+98 51 3884 8930

Outcome results

None listed

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