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Effectiveness of simvastatin on multiple sclerosis (MS)

Phase 2
Conditions
Multiple sclerosis.
Multiple sclerosis
Registration Number
IRCT2015112925284N1
Lead Sponsor
Vice Chancellor for Research, Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Relapsing-remitting MS patients; at least 1 relapse in the previous 12 months; more than three lesions on spinal or brain magnetic resonance imaging or both; baseline expanded disability status scale (EDSS) from 0 to 3.5; aged 18–60 years.
Exclusion criteria: clinical CIS syndrome, progressive MS, MS patients with acute clinical relapses occurring during the study, drug abuse, renal failure, pregnancy, hepatitis diseases.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Assay of cell amplification of peripheral blood luokocytes. Timepoint: 6 months after entering the intervention. Method of measurement: MTT assay.
Secondary Outcome Measures
NameTimeMethod
evel of cytokines. Timepoint: 6 months after entering the intervention. Method of measurement: ELISA.
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