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The effect of cerebrolysin versus placebo on improvement of patients with acute ischemic stroke

Phase 2
Conditions
Ichemic stroke.
cerebral infarction
Registration Number
IRCT201406169014N36
Lead Sponsor
Vice-chancellor for Research the Technology, Hamadan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
122
Inclusion Criteria

(a) having ischemic stroke; (b) age of 40 to 85 years; (c) referring the patient within less than 24 hours after stroke.

Exclusion criteria: (a) being in coma; (b) having systolic blood pressure above 240 mmHg or diastolic blood pressure above 120 mmHg; (c) history of myocardial infarction or heart failure; (d) history of renal failure; (e) history of liver failure; (f) having severe dementia.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Measuring motor function. Timepoint: before intervention and 3 and 7 days after intervention. Method of measurement: using Canadian Stroke Scale.
Secondary Outcome Measures
NameTimeMethod
Measuring motor function. Timepoint: one month after intervention. Method of measurement: using Madified Ranking Scale.;Measuring motor function. Timepoint: one month after intervention. Method of measurement: using Bartel Index.
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