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Topiramate for migraine prevention: a randomized controlled trial
Jan Lewis Brandes1, Joel R Saper, Merle Diamond
1Nashville Neuroscience Group, Nashville, Tenn 37203, USA. jbrandes@nashvilleneuroscience.com
Topiramate significantly reduced monthly migraine frequency and days within the first month of treatment, demonstrating sustained efficacy for migraine prevention in a large controlled trial.
Area of Science:
- Neurology
- Clinical Pharmacology
Background:
- Previous trials indicated topiramate's potential for migraine prevention.
- This study aimed to confirm its efficacy and safety in a larger population.
Purpose of the Study:
- To evaluate the efficacy and safety of topiramate for preventing migraines in a large-scale, randomized, double-blind, placebo-controlled trial.
Main Methods:
- A 26-week trial randomized 483 patients (aged 12-65) with a history of migraines to receive placebo or topiramate (50, 100, or 200 mg/d).
- Topiramate was titrated over 8 weeks, followed by 18 weeks of maintenance treatment.
- Primary endpoint was the change in mean monthly migraine frequency; secondary endpoints included responder rates and reduction in migraine days.
Main Results:
- Topiramate at 100 and 200 mg/d significantly reduced monthly migraine frequency compared to placebo (P<.001).
- Responder rates were significantly higher across all topiramate doses (50, 100, 200 mg/d) versus placebo (P<.001).
- Significant reductions in migraine days and rescue medication use were observed with 100 and 200 mg/d topiramate.
Conclusions:
- Topiramate demonstrated significant efficacy for migraine prevention, with effects observed within the first month of treatment.
- The preventive effect of topiramate was maintained throughout the 26-week study duration.
- Common adverse events leading to discontinuation included paresthesia, fatigue, and nausea.
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