Effects of atorvastatin in traumatic brain injury
Not Applicable
- Conditions
- traumatic brain injury.intracranial injury
- Registration Number
- IRCT2013041910178N5
- Lead Sponsor
- Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
all patients with traumatic brain injury exclusion criteria: hemorrhagic stroke; sensitivity to memantine; acute or chronic renal failure; acute or chronic hepatic disease; acute MI (<48 hours); autoimmune diseases; administration of atorvastatin during 6 months before stroke
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method euron specific enolase. Timepoint: Day 1,3,5. Method of measurement: Elisa kits.
- Secondary Outcome Measures
Name Time Method Glasgow Coma scale. Timepoint: fraom day 1 for 7days. Method of measurement: GCS chart.;Mortality. Timepoint: 90 days after trauma. Method of measurement: Will be checked by phone.