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comparison of Fingolimode and Betaferon(high dose) in M.S treatment

Not Applicable
Conditions
M.S.
Multiple Sclerosis
Registration Number
IRCT2015112025146N1
Lead Sponsor
Isfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
50
Inclusion Criteria

The most important one is MS patients who had treatment failure (relapsing rate more than one) under Betaferon ( low dose) ; patient acceptance; non immunosuppressive patient.
Exclusion criteria: noncooperative patient; death

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Disability Status. Timepoint: befor intervention and 3.9.12.18 months after intervention. Method of measurement: Check list of E.D.S.S.;Relapse Numbers. Timepoint: 0,3,9,12,18 months after intervention. Method of measurement: History and observation.
Secondary Outcome Measures
NameTimeMethod
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