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Evaluation of clarithromycin on TNF-a serum level in patients with multiple sclerosis

Phase 2
Recruiting
Conditions
Multiple sclerosis.
Multiple sclerosis
Registration Number
IRCT20100119003106N41
Lead Sponsor
Islamic Azad University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
28
Inclusion Criteria

Age of 20 t 60 years
Confirmed diagnosis of primary progressive progressive MS
No medical history of allergy to clarithromycin

Exclusion Criteria

Pregnancy or breast feeding patients
Serious underlying medical conditions (e.g malignancy, renal and hepatic failure)
Known hypersensitivity to clarithromycin and excipients
Significant signs of depression

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
TNF-a. Timepoint: Before intervention and 2, 6, 8 weeks after intervention. Method of measurement: ELISA Kit.;Quality of life. Timepoint: before intervention and 2, 6, 8 weeks after intervention. Method of measurement: The quality of life questionnaire.
Secondary Outcome Measures
NameTimeMethod
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