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The effect of intravenous sodium valproate versus dexamethasone on acute migraine headache

Phase 3
Conditions
Acute migraine headache.
Migraine with or without aura
Registration Number
IRCT201202199014N1
Lead Sponsor
Vic-Chancellor of Research and Technology, Hamadan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
72
Inclusion Criteria

Age of 18 to 65 years; history of having migraine for at least one year; severity of headache equal to or greater than 5 VAS

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of headache. Timepoint: At baseline and then 0.5 hour and 2 hours later. Method of measurement: Visual Analogue Scale (VAS).
Secondary Outcome Measures
NameTimeMethod
Any side effect such as allergy. Timepoint: 0.5 hour and 2 hours later. Method of measurement: Questionnaire.
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