Comparison the effect of propofol with subcutaneous Sumatriptane in treatment of acute migraine headache
Not Applicable
- Conditions
- Migraine.G43.0,G43.Migraine without aura [common mMigrain)migrane with aura [classical migraine]igraine],
- Registration Number
- IRCT201008174583N1
- Lead Sponsor
- Shahid Sadoughi University of Medical Sciences-Yazd, Iran
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
all patients aged between 18 and 45 years old with acute migraine headache admitted in emergency department or pain clinic.
exclusion criteria are pregnancy; opium addiction; diastolic pressure greater than 105. Sign and symptoms of organic headache peripheral and coronary artery disease.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Headache severity. Timepoint: Before intervention; half an hour; one hour; and 2 hours after intervention. Method of measurement: Visual Analog Scale(VAS).
- Secondary Outcome Measures
Name Time Method Accompanying symptoms including nausea vomiting photophobia and phonophobia. Timepoint: Before, half an hour, and one hour after intervention. Method of measurement: Observation.;Drug side effects including hypotension; bradycardia; nausea; vertigo; paresthesia. Timepoint: After intervention. Method of measurement: Observation.