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Evaluation the effect of adding methylprednisolone to mitoxantrone on progressive multiple sclerosis treatment

Not Applicable
Conditions
Multiple Sclerosis.
Demyelinating diseases of the central nervous system
Registration Number
IRCT201107145943N3
Lead Sponsor
Yazd University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
70
Inclusion Criteria

presence of progressive MS, age between 20 to 50
Exclusion criteria: Age below 20 or above 50, Immune deficiency, cancer, Pregnancy or breast feeding, Renal or heart failure, Leukopenia during the injection (the reduction of neutrophils to less than 1500/ml), having received corticosteroids within 6 months before the trial

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
MRI plaque numbers. Timepoint: 6 months and 1 year after the intervention. Method of measurement: Based on MRI imaging.;Expanded Disability Status Scale (EDSS). Timepoint: 6 months and 1 year after the intervention. Method of measurement: Based on definit idex.
Secondary Outcome Measures
NameTimeMethod
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