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一项评估50毫克舒马曲坦片在偏头痛急性治疗中的疗效和耐受性的双盲安慰剂对照研究。舒马曲坦片S2CM07研究组。

A double-blind placebo-controlled study assessing the efficacy and tolerability of 50 mg sumatriptan tablets in the acute treatment of migraine. Sumatriptan Tablets S2CM07 Study Group.

作者信息

Savani N, Brautaset N J, Reunanen M, Szirmai I, Ashford E A, Hassani H, Saiers J

机构信息

Semmelweiss Medical University, Budapest, Hungary,

出版信息

Int J Clin Pract Suppl. 1999 Aug;105:7-15.

Abstract

BACKGROUND

Oral sumatriptan 50 mg has been found to have good efficacy and tolerability in the acute treatment of migraine but has been less well studied than the 100 mg dose.

METHODS

This was a double-blind, parallel-group study (Glaxo Wellcome protocol number S2CM07) comparing the efficacy and safety of sumatriptan 50 mg tablets with placebo in the acute treatment of migraine. Patients treated three migraine attacks with study medication; a second, optional dose was available for treating recurrent headache. Of the 560 patients randomized, 485 treated at least one attack, 411 at least two attacks, and 362 three attacks. The primary efficacy measure was the proportion of patients who had obtained complete or almost complete headache relief at 4 h after dosing.

RESULTS

For all attacks, a significantly greater proportion of patients experienced headache relief at 4 h with sumatriptan 50 mg tablets than with placebo (59% to 62% versus 32% to 42%; P = 0.005). The same was true at 3 h across all attacks, and at 2 h for attacks 1 and 2 (49% versus 23% and 45% versus 29%, respectively). Although sumatriptan and placebo were associated with similar incidences of recurrence, sumatriptan was associated with a longer time to recurrence. The incidence of adverse events with sumatriptan was similar to that with placebo, and there was no increase in adverse events associated with use of a second dose to treat recurrence.

CONCLUSIONS

Sumatriptan 50 mg tablets are well tolerated and efficacious in relieving migraine headache.

摘要

背景

已发现口服50毫克舒马曲坦在偏头痛急性治疗中具有良好的疗效和耐受性,但与100毫克剂量相比,其研究较少。

方法

这是一项双盲、平行组研究(葛兰素威康协议编号S2CM07),比较50毫克舒马曲坦片剂与安慰剂在偏头痛急性治疗中的疗效和安全性。患者用研究药物治疗三次偏头痛发作;有第二个可选剂量用于治疗复发性头痛。在随机分组的560例患者中,485例治疗了至少一次发作,411例治疗了至少两次发作,362例治疗了三次发作。主要疗效指标是给药后4小时获得完全或几乎完全头痛缓解的患者比例。

结果

对于所有发作,服用50毫克舒马曲坦片剂的患者在4小时时头痛缓解的比例显著高于服用安慰剂的患者(59%至62%对32%至42%;P = 0.005)。在所有发作的3小时时以及发作1和2的2小时时情况相同(分别为49%对23%和45%对29%)。虽然舒马曲坦和安慰剂的复发率相似,但舒马曲坦的复发时间更长。舒马曲坦的不良事件发生率与安慰剂相似,并且使用第二个剂量治疗复发并未增加不良事件。

结论

50毫克舒马曲坦片剂耐受性良好,对缓解偏头痛有效。

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