Comparison of the effect of intravenous paracetamol (Apotel) and dexamethasone in the relief of acute migraine headaches
Phase 3
Recruiting
- Conditions
- Acute migraine headache.Cluster headache syndrome, unspecifiedG44.0
- Registration Number
- IRCT20240619062184N1
- Lead Sponsor
- Birjand University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Not having a specific neurological disease
No history of continuous use of drugs and long-term painkillers
Exclusion Criteria
pregnancy
History of neurological disease
Patients without personal consent
Having a body temperature higher than37.7 degrees Celsius
Having a diastolic blood pressure greater than 105 mm Hg
Patients treated with systemic corticosteroids
Allergy to dexamethasone, egg and soy
Patients with a history of diabetes mellitus
Active gastrointestinal ulcers
Myocardial infarction in the previous week
Hypokalemic familial paralysis (for dexamethasone)
Continuous use of drugs and long-term painkillers
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain reduction in acute migraine headache patients based on Visual pain measurement criteria. Timepoint: When the patient enters the study. Method of measurement: Visual pain measurement criteria.
- Secondary Outcome Measures
Name Time Method