首页> 美国卫生研究院文献>Springer Open Choice >Efficacy of frovatriptan versus other triptans in the acute treatment of menstrual migraine: pooled analysis of three double-blind randomized crossover multicenter studies
【2h】

Efficacy of frovatriptan versus other triptans in the acute treatment of menstrual migraine: pooled analysis of three double-blind randomized crossover multicenter studies

机译:曲伐曲普坦与其他曲普坦在月经性偏头痛急性治疗中的功效:三项双盲随机交叉多中心研究的综合分析

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The objective of this study was to review the efficacy and safety of frovatriptan (F) versus rizatriptan (R), zolmitriptan (Z) and almotriptan (A), in women with menstrually related migraine (IHS criteria) through a pooled analysis of three individual studies. Subjects with a history of migraine with or without aura were randomized to F 2.5 mg or R 10 mg (study 1), F or Z 2.5 mg (study 2), and F or A 12.5 mg (study 3). The studies had an identical multicenter, randomized, double-blind, crossover design. After treating three episodes of migraine in no more than 3 months with the first treatment, patients had to switch to the next treatment for other 3 months. 346 subjects formed intention-to-treat population of the main study; 280 of them were of a female gender, 256 had regular menses and 187 were included in the menstrual migraine subgroup analysis. Rate of pain free at 2, 4 and 24 h was 23, 52 and 67 % with F and 30, 61 and 66 % with comparators (P = NS). Pain relief episodes at 2, 4 and 24 h were 37, 60 and 66 % for F and 43, 55 and 61 % for comparators (P = NS). Rate of recurrence was significantly (P < 0.05) lower under F either at 24 h (11 vs. 24 % comparators) or at 48 h (15 vs. 26 % comparators). Number of menstrual migraine attacks associated with drug-related adverse events was equally low (P = NS) between F (5 %) and comparators (4 %).
机译:这项研究的目的是通过对三个个体的合并分析,复查佛罗曲坦(F)相对于利扎曲普坦(R),佐米曲普坦(Z)和阿莫曲普坦(A)在月经相关偏头痛妇女中的疗效和安全性(IHS标准)学习。有偏头痛史或无先兆史的受试者被随机分为F 2.5 mg或R 10 mg(研究1),F或Z 2.5 mg(研究2),F或A 12.5 mg(研究3)。这些研究具有相同的多中心,随机,双盲,交叉设计。第一次治疗在不超过3个月内治疗了3次偏头痛发作后,患者不得不改用其他3个月的下一个治疗方法。 346名受试者组成了主要研究的意向性治疗人群;其中280例为女性,256例为常规月经,187例被纳入月经偏头痛亚组分析。 F,2、4和24小时的无痛率为23%,52%和67%,而比较者为30%,61%和66%(P = NS)。 F,2、4和24小时的疼痛缓解发作分别为37%,60%和66%,而比较者的疼痛缓解发作分别为43%,55%和61%(P = NS)。在24小时(11%vs.24%的比较者)或48小时(15%vs.26%的比较者)下,F下的复发率显着降低(P <0.05)。在F(5%)和比较者(4%)之间,与药物相关的不良事件相关的月经偏头痛发作次数同样较低(P = NS)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号