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The effect of salimarin in patients with multiple sclerosis

Phase 2
Conditions
Condition 1: Multiple Sclerosis. Condition 2: Liver disease.
Multiple sclerosis
Other diseases of liver
Registration Number
IRCT20150628022956N7
Lead Sponsor
Research Council of Hamedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
48
Inclusion Criteria

Patients who have had at least 3 weeks of onset of corticosteroid attack and received corticosteroids with liver enzymes following corticosteroid therapy.
New Patients Receive Fingolimod
Patients who are taking interferon and Glatiramer are advised to take the Fingolimod, provided they have no liver problem.
Expanded Disability Status Scale below three.

Exclusion Criteria

Pregnant and lactating women
Patients who are allergic to Silymarin
Patients with previous history of tuberculosis, HIV, hepatitis and liver problems.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
iver complications. Timepoint: At the beginning of the study (before the intervention) and 30, 60, 90, 120, 150 and 180 days after taking Silymarin. Method of measurement: Malondialdehyde index with Ohkawa method- Total antioxidant capacity index with FRAP method- Measurement of protein thiol groups with Ellman's Reagent (DTNB).
Secondary Outcome Measures
NameTimeMethod
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