Comparison of the efficacy of intravenous sodium valproate and acetaminophen in attacks of headaches
Phase 2
Recruiting
- Conditions
- Migraine headach.Migraine
- Registration Number
- IRCT20141209020258N102
- Lead Sponsor
- Arak University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
Normal systemic and neurological examinations
20 to 50 yeras
Exclusion Criteria
Allergy to acetaminophen
Hyperammonium
Lack of cooperation
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: One and six hours after the start of the study. Method of measurement: Visual analog scale.
- Secondary Outcome Measures
Name Time Method