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Valproate Versus Topiramate in Migraine, a Randomized Controlled Trial
Investigators aim to compare the effect of valproate versus topiramate in migraine by assessing the reduction in MMD in each group, the percentage of patients who achieved ≥ 50% reduction in the monthly headache days frequency compared to the baseline frequency.
Investigators will enroll 600 migraine patients who are diagnosed according to ICHD3-beta criteria in our study and will use a questionnaire to detect their demographic and clinical features (disease duration, attack frequency, and duration, pain intensity assessed by the visual analogic scale and we have two groups the first group will include 300 patients and will receive 500-1000mg valproate daily and Acetaminophen 500-1000 mg in acute attack, and the second group will receive topiramate100 mg per day and Acetaminophen 500-1000 mg in acute attack for at least three months. Investigators will assess The number of migraine days after three months of treatment and the percentage of patients who achieved ≥ 50% reduction in the monthly headache days frequency compared to the baseline frequency (14).. HIT-6 score reduction in each group after three months of treatment. The safety of treatment was evaluated by monitoring and documenting treatment-emergent adverse events (TEAE) in patients through regular follow-up procedures for three months.
Age
18 - 55 years
Sex
ALL
Healthy Volunteers
No
Kafr Elsheikh University Hospital
Kafr ash Shaykh, Egypt
Start Date
May 1, 2022
Primary Completion Date
June 10, 2024
Completion Date
June 30, 2024
Last Updated
July 15, 2024
600
ACTUAL participants
Valproic acid
DRUG
Topiramate 50 MG
DRUG
Lead Sponsor
Kafrelsheikh University
Data Source & Attribution
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View ClinicalTrials.gov Terms and ConditionsNCT05690737