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Effect of Sylimarin versus placebo on the reduction of liver complication of Teriflunomide in patients with multiple sclerosis

Phase 3
Recruiting
Conditions
Multiple sclerosis.
Multiple sclerosis
Registration Number
IRCT20120215009014N467
Lead Sponsor
Hamedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
42
Inclusion Criteria

Age 18 to 70 years
Multiple sclerosis

Exclusion Criteria

Pregnancy or breastfeeding
Alcohol consumption
Active viral hepatitis or chronic liver disease

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
iver and biliary function tests (including AST, ALT, ALP, bilirubin and GGT). Timepoint: Before the intervention and one and two months after the intervention. Method of measurement: By laboratory test.
Secondary Outcome Measures
NameTimeMethod
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