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首页> 外文期刊>Neurological sciences >Efficacy of frovatriptan versus other triptans in the acute treatment of menstrual migraine: pooled analysis of three double-blind, randomized, crossover, multicenter studies.
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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:弗罗曲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,多中心研究的汇总分析。

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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?
机译:这项研究的目的是通过对三名个体进行月经量测的综合分析,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)的疗效和安全性学习。有偏头痛史或无先兆病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)和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个月的时间内治疗了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。在F,2、4和24?h时,无痛的发生率分别为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%,而比较者为43%,55%和61%(P == NS)。在24?h(11%vs. 24 %%的比较者)或48?h(15%vs. 26 %%的比较者)下,F下的复发率显着降低(P <0.05)。在F(5%)和对照者(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)。

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