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The Effects of Filgrastim on Prognosis of Patients with acute Ischemic Stroke

Phase 2
Recruiting
Conditions
acute Ischemic Stroke.
Cerebral infarction, unspecified
Registration Number
IRCT20141209020258N63
Lead Sponsor
Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
84
Inclusion Criteria

18 years and more
Patients with acute ischemic stroke

Exclusion Criteria

Drinking alcohol and addict
Incidence of side effects or the sensitivity of the drug
History of blood pressure, diabetes, embolism and DVT
Death of the patient 72 hours after entering the emergency room

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hemoglobin. Timepoint: Before and during treatment and 4 weeks after treatment. Method of measurement: blood test.;Power of the paraplegic organ. Timepoint: Before and during treatment and 4 weeks after treatment. Method of measurement: Physical examination.;Awareness status. Timepoint: Before and during treatment and 4 weeks after treatment. Method of measurement: Glasgow Coma Scale.;Motion status. Timepoint: Before and during treatment and 4 weeks after treatment. Method of measurement: Physical examination.;Hematocrit. Timepoint: Before and during treatment and 4 weeks after treatment. Method of measurement: blood test.
Secondary Outcome Measures
NameTimeMethod
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