Topiramate in migraine prophylaxis -: Results from a placebo-controlled trial with propranolol as an active control

被引:301
作者
Diener, HC
Tfelt-Hansen, P
Dahlöf, C
Láinez, MJA
Sandrini, G
Wang, SJ
Neto, W
Vijapurkar, U
Doyle, A
Jacobs, D
机构
[1] Univ Essen Gesamthsch, Dept Neurol, D-45122 Essen, Germany
[2] Univ Copenhagen, Glostrup Hosp, Dept Neurol, Glostrup, Denmark
[3] Gothenburg Migraine Clin, Gothenburg, Sweden
[4] Univ Valencia, Hosp Clin Univ, Dept Neurol, Valencia, Spain
[5] Univ Pavia, IRC C Mondino Fdn, Headache Ctr, I-27100 Pavia, Italy
[6] Taipei Vet Gen Hosp, Neurol Inst, Taipei, Taiwan
[7] Natl Yang Ming Univ, Sch Med, Taipei 112, Taiwan
[8] Johnson & Johnson Pharmaceut Res & Dev LLC, Raritan, NJ USA
关键词
placebo-controlled; migraine; topiramate; prophylaxis; propranolol;
D O I
10.1007/s00415-004-0464-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Topiramate (TPM) has shown efficacy in migraine prophylaxis in two large placebo-controlled, dose-ranging trials. We conducted a randomised, double-blind, multicentre trial to evaluate the efficacy and safety of two doses of topiramate vs placebo for migraine prophylaxis, with propranolol (PROP) as an active control. Subjects with episodic migraine with and without aura were randomised to TPM 100 mg/d, TPM 200 mg/d, PROP 160 mg/d (active control), or placebo. The primary efficacy measure was the change in mean monthly migraine frequency from the baseline phase relative to the double-blind treatment phase. Five hundred and seventy-five subjects were enrolled from 61 centres in 13 countries. TPM 100 mg/d was superior to placebo as measured by reduction in monthly migraine frequency, overall 50% responder rate, reduction in monthly migraine days, and reduction in the rate of daily rescue medication use. The TPM 100 mg/d and PROP groups were similar with respect to reductions in migraine frequency, responder rate, migraine days, and daily rescue medication usage. TPM 100 mg/d was better tolerated than TPM 200 mg/d, and was generally comparable to PROP. No unusual or unexpected safety risks emerged. These findings demonstrate that TPM 100 mg/d is effective in migraine prophylaxis. TPM 100 mg/d and PROP 160 mg/d exhibited similar efficacy profiles.
引用
收藏
页码:943 / 950
页数:8
相关论文
共 16 条
  • [1] Topiramate for migraine prevention - A randomized controlled trial
    Brandes, JL
    Saper, JR
    Diamond, M
    Couch, JR
    Lewis, DW
    Schmitt, J
    Neto, W
    Schwabe, S
    Jacobs, D
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 291 (08): : 965 - 973
  • [2] One-year prevalence of migraine in Sweden:: a population-based study in adults
    Dahlöf, C
    Linde, M
    [J]. CEPHALALGIA, 2001, 21 (06) : 664 - 671
  • [3] DIENER HC, 2003, COURSE TREATMENT NEU, P1
  • [4] Edwards K. R., 2000, Cephalalgia, V20, P316
  • [5] A randomized trial of divalproex sodium extended-release tablets in migraine prophylaxis
    Freitag, FG
    Collins, SD
    Carlson, HA
    Goldstein, J
    Saper, J
    Silberstein, S
    Mathew, N
    Winner, PK
    Deaton, R
    Sommerville, K
    [J]. NEUROLOGY, 2002, 58 (11) : 1652 - 1659
  • [6] Drug therapy: Migraine - Current understanding and treatment.
    Goadsby, PJ
    Lipton, RB
    Ferrari, MD
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (04) : 257 - 270
  • [7] Clinical features of withdrawal headache following overuse of triptans and other headache drugs
    Katsarava, Z
    Fritsche, G
    Muessig, M
    Diener, HC
    Limmroth, V
    [J]. NEUROLOGY, 2001, 57 (09) : 1694 - 1698
  • [8] Divalproex sodium in migraine prophylaxis: A dose-controlled study
    Klapper, J
    [J]. CEPHALALGIA, 1997, 17 (02) : 103 - 108
  • [9] MIGRAINE PROPHYLAXIS WITH DIVALPROEX
    MATHEW, NT
    SAPER, JR
    SILBERSTEIN, SD
    RANKIN, L
    MARKLEY, HG
    SOLOMON, S
    RAPOPORT, AM
    SILBER, CJ
    DEATON, RL
    [J]. ARCHIVES OF NEUROLOGY, 1995, 52 (03) : 281 - 286
  • [10] MIGRAINE WITH AURA AND MIGRAINE WITHOUT AURA - AN EPIDEMIOLOGIC-STUDY
    RASMUSSEN, BK
    OLESEN, J
    [J]. CEPHALALGIA, 1992, 12 (04) : 221 - 228