Comparison of analgesic effect of Paracetamol with combination of Paracetamol and Propofol in the relief of acute migraine headache
Phase 3
Recruiting
- Conditions
- Acute migraine headache.Migraine
- Registration Number
- IRCT20180628040274N1
- Lead Sponsor
- Zahedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Failure to receive narcotic drugs or other Triptans, such as vasoconstrictor, such as Dihydroergotamine, within 24 hours before referral to the emergency department
Patients treated with systemic Corticosteroids
Patients with Diabetes Mellitus history, active gastrointestinal ulcers, myocardial infarction in the last week
Family history of hypocalmic paralysis (for Dexamethasone)
Exclusion Criteria
Those who have kidney failure
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: Pain score is recorded based on the VAS scale before treatment and 5, 10, 20, 30, and 45 minutes after treatment. Method of measurement: By VAS or Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method