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The effect of erythropoetin on Multiple Sclerosis

Not Applicable
Conditions
Multiple sclerosis.
Multiple sclerosis
Registration Number
IRCT2013081914407N1
Lead Sponsor
Tehran university of medical science research assistance
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
20
Inclusion Criteria

definite diagnosis of MS; age between 18 and 45 years old and motor force 3/5 or less at presentation.
Exclusion criteria: pregnancy; brestfeeding; history of diabetes mellitus, hypertension, hyperlipidmia, heavy cigarette smoking, ischemic heart disease, myocardial infarction, cerebovasculaar accident; family history of ischemic heart disease and /or cerebrovascular accident before 45 years; presence of thrombocytosis; presence of polycytemia(hematocrite above 50% in males and above 45% in females); presence of CRF(chronic renal failure); history of any vasculitis or collagen vascular disease; use of contraceptive medication; use of iron substitution; past history of thromboembololic events and any kind of malignancy(treated or untreated).

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
EDSS. Timepoint: Before intervention, one, two three months after intervention. Method of measurement: Examination.;Ambulatory Index. Timepoint: Before intervention, one, two three months after intervention. Method of measurement: Examination.;MRI. Timepoint: Before intervention and three months after intervention. Method of measurement: Visual.
Secondary Outcome Measures
NameTimeMethod
Blood Pressure. Timepoint: Before intervention, five day and one and three months after intervention. Method of measurement: Sphygmomanometer.;RBC count. Timepoint: Before intervention, five day and three months after intervention. Method of measurement: Laboratory.
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