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Ellagic acid in multiple sclerosis

Effect of Ellagic acid supplementation on disease severity, expression of involved genes in pathogenesis, and levels of immunity and inflammatory biomarkers in patients with Multiple Sclerosis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120415009472N22
Enrollment
46
Registered
2020-12-19
Start date
2021-01-10
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Multiple Sclerosis. Multiple sclerosis

Interventions

Intervention 1: Intervention group: Intervention group: The intervention group receives two 90 mg capsules of ellagic acid daily for 12 weeks before lunch and dinner (made by Exir Gostar Company). Int

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Patient informed consent Disease diagnosis based on McDonald's criteria and MRI by a neurologist EDSS score less than 5.5 Relapsing-remitting status of the disease age between 18 and 55 years

Exclusion criteria

Exclusion criteria: Reluctance to participate in the study Take nutritional supplements, antioxidants, and ellagic acid during a month before the start of the study and during the study (except for routine supplements that are part of the treatment plan for all patients, including vitamin D) Taking nonsteroidal anti-inflammatory drugs, estrogen, progesterone, immunosuppressives, diuretics, and corticosteroids during a month before the study Patients with inflammatory bowel disease (IBD), rheumatoid arthritis, systemic lupus erythematosus, type 1 diabetes, and other autoimmune diseases are excluded from the study. Pregnancy and lactation Drug abuse

Design outcomes

Primary

MeasureTime frame
Expanded Disability Status Scale. Timepoint: At the beginning of the study and 12 weeks after supplementation with ellagic acid. Method of measurement: Extensive Disability Scale Questionnaire.

Secondary

MeasureTime frame
Interleukin 17. Timepoint: At the beginning of the study and 12 weeks after supplementation with ellagic acid. Method of measurement: Interleukin 17 kit by ELISA method.;Interleukin 4. Timepoint: At the beginning of the study and 12 weeks after supplementation with ellagic acid. Method of measurement: Interleukin 4 kit by ELISA method.;Transforming growth factor beta (TGF-ß). Timepoint: At the beginning of the study and 12 weeks after supplementation with ellagic acid. Method of measurement: TGF-ß kit by ELISA method.;Interferon gamma. Timepoint: At the beginning of the study and 12 weeks after supplementation with ellagic acid. Method of measurement: Interferon gamma kit by ELISA method.;T-bet gene expression. Timepoint: At the beginning of the study and 12 weeks after supplementation with ellagic acid. Method of measurement: Standard quantitative real - time PCR.;GATA3 gene expression. Timepoint: At the beginning of the study and 12 weeks after supplementation with ellagic acid. Method of measurement: Standard quantitative real - time PCR.;ROR?t gene expression. Timepoint: At the beginning of the study and 12 weeks after supplementation with ellagic acid. Method of measurement: Standard quantitative real - time PCR.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Naheed Aryaeian

Iran University of Medical Sciences

nah_arya2002@yahoo.com+98 21 8670 4750

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 8, 2026