Effect of L-carnitine inpatients with traumatic brain injury
Phase 3
- Conditions
- Traumatic Brain Injury.Cerebral oedema traumatic (S06.1)
- Registration Number
- IRCT201410312582N9
- Lead Sponsor
- Research deputy of Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Patients aging 18-75 years with traumatic brain injury in last 24 hours
Exclusion criteria:having brain trauma in more than previous 24 hours; diarrhea; abdominal cramps; patients with kidney failure undergoing dialysis; history of heart disease; history of sensitivity to L-carnitine; having other traumas such as organic trauma; hypertension; alcoholic cirrhosis
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Glascow Coma Scale(GCS). Timepoint: 1 week. Method of measurement: assay with GCS(Eye opening, limb movement, verbal).
- Secondary Outcome Measures
Name Time Method