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2.5毫克佐米曲普坦用于偏头痛急性治疗的临床疗效和耐受性。042临床试验研究组。

Clinical efficacy and tolerability of 2.5 mg zolmitriptan for the acute treatment of migraine. The 042 Clinical Trial Study Group.

作者信息

Solomon G D, Cady R K, Klapper J A, Earl N L, Saper J R, Ramadan N M

机构信息

Cleveland Clinic Foundation, OH, USA.

出版信息

Neurology. 1997 Nov;49(5):1219-25. doi: 10.1212/wnl.49.5.1219.

DOI:10.1212/wnl.49.5.1219
PMID:9371897
Abstract

Previous studies demonstrated that zolmitriptan at doses of 1 to 25 mg was highly effective in treating acute migraine attacks. The 2.5-mg dose had a favorable therapeutic effect with high efficacy and good tolerability. The objective of this study was to further evaluate the efficacy of a single 2.5-mg dose of zolmitriptan (Zomig, formerly known as 311C90) for acute treatment of a single moderate or severe migraine attack. The study was a randomized, double-blind, placebo-controlled clinical trial. Female and male patients, 12 to 65 years old, with migraine (with or without aura) for > or = 1 year, one to six migraines per month, and age at onset < 50 years were included; 327 patients were screened and randomized to receive either zolmitriptan (n = 219) or placebo (n = 108). Patients treated a single moderate or severe migraine headache with 2.5 mg zolmitriptan or placebo and recorded clinical efficacy and adverse events on a diary form. Headache response at 2 hours was 62% for zolmitriptan compared with 36% for placebo (p < 0.001); at 4 hours, headache response was 70% with zolmitriptan and 37% with placebo (p < 0.001). Headache recurrence in patients treated with 2.5 mg zolmitriptan was 22% (versus placebo 30%). The headache response at 4 hours, pain-free rate, and response rate of nonheadache symptoms favored zolmitriptan over placebo. No serious adverse events were associated with zolmitriptan treatment. A 2.5-mg dose of zolmitriptan is clinically effective and well tolerated for the acute treatment of migraine.

摘要

以往研究表明,1至25毫克剂量的佐米曲坦在治疗急性偏头痛发作方面非常有效。2.5毫克剂量具有良好的治疗效果,疗效高且耐受性好。本研究的目的是进一步评估单次2.5毫克剂量的佐米曲坦(佐米格,原名311C90)用于急性治疗单次中度或重度偏头痛发作的疗效。该研究是一项随机、双盲、安慰剂对照的临床试验。纳入年龄在12至65岁之间、患有偏头痛(有或无先兆)≥1年、每月发作1至6次偏头痛且发病年龄<50岁的女性和男性患者;327名患者经过筛选并随机分为接受佐米曲坦治疗组(n = 219)或安慰剂组(n = 108)。患者使用2.5毫克佐米曲坦或安慰剂治疗单次中度或重度偏头痛头痛,并通过日记形式记录临床疗效和不良事件。佐米曲坦组在2小时时的头痛缓解率为62%,而安慰剂组为36%(p < 0.001);在4小时时,佐米曲坦组的头痛缓解率为70%,安慰剂组为37%(p < 0.001)。接受2.5毫克佐米曲坦治疗的患者头痛复发率为22%(而安慰剂组为30%)。在4小时时的头痛缓解情况、无痛率以及非头痛症状的缓解率方面,佐米曲坦优于安慰剂。佐米曲坦治疗未出现严重不良事件。2.5毫克剂量的佐米曲坦在偏头痛急性治疗中临床疗效显著且耐受性良好。

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