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Ellagic acid in multiple sclerosis

The effect of Ellagic acid on depression, inflammatory index (IFN-?), oxidative (Nrf2) and nitrosative (NO) stress index, Brain Derived Neurotrophic Factor (BDNF), cortisol, serotonin and gene expression of indoleamine dioxygenase enzyme in patients with multiple sclerosis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20091114002709N54
Enrollment
46
Registered
2020-06-07
Start date
2020-08-05
Completion date
Unknown
Last updated
2020-06-15

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: The intervention group receives two 90 mg allagic acid capsules daily for 12 weeks before lunch and dinner. Intervention 2: Control group: The placebo group takes t

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Willingness to cooperate Age range 18 to 55 years Depression according to Beck's questionnaire (score above 10) No change in the dose of antidepressant medication in the last three months Diagnosis of MS by a neurologist Patients are at recurrence and recovery EDSS <5.5

Exclusion criteria

Exclusion criteria: Take nutritional, antioxidant, and ellagic acid supplements for a month before the study (except for routine supplements, which are part of the treatment plan for all patients, such as vitamin D) Pregnancy and lactation Drug abuse History of diabetes and other chronic diseases History of other autoimmune diseases Occurrence of recurrence of the disease during study Taking corticosteroids, estrogens, progesterone, immunosuppressants, diuretics during last month Dose changes and the type of medication used during study Change in physical activity Acceptance rate of less than 90% of supplementation Lack of willingness to cooperate

Design outcomes

Primary

MeasureTime frame
IFN-?. Timepoint: At the beginning and end of the intervention. Method of measurement: Laboratory kit.

Secondary

MeasureTime frame
Depression score. Timepoint: The beginning and the end of the intervention. Method of measurement: Beck questionnaire.;Nrf2. Timepoint: The beginning and end of the intervention. Method of measurement: Laboratory kit.;NO. Timepoint: The beginning and end of the intervention. Method of measurement: Laboratory kit.;BDNF. Timepoint: The beginning and the end of the intervention. Method of measurement: Laboratory kit.;Cortisol. Timepoint: The beginning and the end of the intervention. Method of measurement: Laboratory kit.;Serotonin. Timepoint: The beginning and the end of the intervention. Method of measurement: Laboratory kit.;IDO gene expression. Timepoint: The beginning and end of the intervention. Method of measurement: Real Time RT-PCR.;EDSS. Timepoint: The beginning and the end of the intervention. Method of measurement: EDSS QUESTIONNAIRE.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarzad Shidfar

Iran University of Medical Sciences

shidfar.f@iums.ac.ir+98 21 86701

Outcome results

None listed

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