Comparative efficacy of Cyproheptadine and Baclofen on spasticity in patients with head trauma
Phase 2
- Conditions
- Head Trauma.Multiple superficial injuries of head
- Registration Number
- IRCT2014041112777N1
- Lead Sponsor
- Vice chancellor for research, Ahvaz Jundishapur University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Patients with diffuse axonal injury without chronic hepatic or renal disease; 15 to 60 years old.
Exclusion criteria: Changing in treatment plan like surgery; drug reactions; drug side effects.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Spasticity. Timepoint: 1, 3, 6, 9, 12, 15 days. Method of measurement: Modified Ashworth Scale.
- Secondary Outcome Measures
Name Time Method Alanine Transaminase (ALT). Timepoint: Weekly. Method of measurement: U/ml.;Blood Urea Nitrogen(BUN). Timepoint: Daily. Method of measurement: Mg/dl.;Aspartate Amino Transferase(AST). Timepoint: Weekly. Method of measurement: U/ml.;Alkaline Phosphatase(ALP). Timepoint: Weekly. Method of measurement: U/ml.;Creatinine. Timepoint: Daily. Method of measurement: Mg/dl.