Comparison of sumatriptan and propofol VS Sumatriptan and placebo in acute migraine
Not Applicable
- Conditions
- Migraine.Migraine without aura (common migraine )G43.2-G43.
- Registration Number
- IRCT2015050422089N1
- Lead Sponsor
- Vice chancellor for research, Shahid Sadoughi university of Medical Science Of Yazd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
all patient aged 18 to 45 years old with migrain headache
Exclusion criteria: Pregnancy, Hypertension, Previous CVA, propofol sensitivity, Sumatriptan sensitivity, coronary artery disease.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: Before intervention, 10-minute iterval after intervention until 1 hour. Method of measurement: Visual pain score.
- Secondary Outcome Measures
Name Time Method Hypoxia. Timepoint: Before intervention, 10- minute interval after intervention until 1 hour. Method of measurement: Pulse oximetry.