DIVALPROEX SODIUM IN MIGRAINE PROPHYLAXIS - A DOSE-CONTROLLED STUDY

Authors
Citation
J. Klapper, DIVALPROEX SODIUM IN MIGRAINE PROPHYLAXIS - A DOSE-CONTROLLED STUDY, Cephalalgia, 17(2), 1997, pp. 103-108
Citations number
8
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
03331024
Volume
17
Issue
2
Year of publication
1997
Pages
103 - 108
Database
ISI
SICI code
0333-1024(1997)17:2<103:DSIMP->2.0.ZU;2-D
Abstract
Objective: To evaluate the efficacy and safety of divalproex sodium (D VPX) when used as prophylactic monotherapy in patients with migraine. Design: Multicenter, double-blind, placebo-controlled, parallel group. Patients were previously untreated or had failed no more than two ade quate trials of prophylactic therapy. During the 4-week (single-blind) baseline, patients received placebo and completed a headache diary. P atients with two or more migraine attacks during the baseline were ran domized to receive a DVPX daily dose of 500, 1000, or 1500 mg, or to p lacebo. The experimental phase (EP) lasted 12 weeks, the first 4 weeks for dose escalation to randomized dose, and the remaining 8 weeks for maintenance at that dose. The primary efficacy variable was 4-week mi graine attack frequency during the EP. Results: One-hundred-and-sevent y-six patients (44 placebo, 132 DVPX) were randomized; 171 provided ef ficacy data and 137 completed the study. During the EP, after adjustme nt for differences in baseline migraine attack frequencies, mean reduc tions in the DVPX groups were 1.7 (500 mg), 2.0 (1000 mg) and 1.7 (150 0 mg) migraine attacks per 4 weeks compared to a mean reduction of 0.5 migraine attacks in the placebo group (p less than or equal to 0.05 v s placebo). Forty-four to 45% of DVPX-treated patients compared to 21% of patients in the placebo group achieved greater than or equal to 50 % reduction in their migraine attack frequencies (p less than or equal to 0.05 vs placebo). The recommended initial dose of DVPX in migraine prophylaxis is 500 mg per day, although some patients may benefit fro m higher doses. Adverse events were similar in the DVPX and placebo tr eatment groups except for nausea, dizziness and tremor, in which incid ence rates were significantly higher in the DVPX 1500 mg group (nausea was also higher in 500 mg group) than in the placebo group. Conclusio n: Divalproex sodium is an effective prophylactic treatment in migrain e and is generally well tolerated.