Propofol plus paracetamol in benign headaches.
Phase 2
- Conditions
- Headache.Headache
- Registration Number
- IRCT20141116019971N4
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Age 18 years and above
Benign headaches
Exclusion Criteria
Suspicious to secondary headaches based on the attending physician's judgment
Abnormal vital signs
Variation in the level of consciousness
Fever
Focal neurologic defficite
Pregnancy
Allergy to the egg yolk, acetaminophen or propofol
Neck stiffness
Hepatic failure an chronic liver disease
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain intensity. Timepoint: 0,10, 20, 30, 60 minutes. Method of measurement: Numeric rating scale.
- Secondary Outcome Measures
Name Time Method Blood pressure. Timepoint: 0,10, 20, 30, 60 minutes. Method of measurement: Blood pressure cuff.;Heart rate. Timepoint: 0,10, 20, 30, 60 minutes. Method of measurement: Cardiac monitoring device.;Oxygen saturation. Timepoint: 0,10, 20, 30, 60 minutes. Method of measurement: Puls oxymeter.