Mathew Ninan T, Schoenen Jean, Winner Paul, Muirhead Nancy, Sikes Carolyn R
Houston (Tex) Headache Clinic, TX 77004, USA.
Headache. 2003 Mar;43(3):214-22. doi: 10.1046/j.1526-4610.2003.03044.x.
To confirm the efficacy advantage of eletriptan 40 mg over sumatriptan 100 mg. Background.-Eletriptan 80 mg has demonstrated significantly greater efficacy when compared to both sumatriptan 50 mg and 100 mg in two studies. Eletriptan 40 mg demonstrated significantly greater efficacy than sumatriptan 100 mg in one previous trial.
Two thousand one hundred thirteen patients with a diagnosis of migraine according to International Headache Society criteria were randomized using a double-blind, double-dummy, parallel-group design, and treated for a single migraine attack with either eletriptan 40 mg, sumatriptan 100 mg, or placebo. The primary endpoint was 2-hour headache response. Secondary endpoints included headache response rates at 1 hour, pain-free rates, absence of associated symptoms, functional response at 1 and 2 hours, and sustained headache response.
Headache response rates at 2 hours postdose were significantly higher for eletriptan 40 mg (67%) than for sumatriptan 100 mg (59%; P <.001) and placebo (26%; P <.0001). Eletriptan 40 mg consistently showed significant (P <.01) efficacy over sumatriptan 100 mg across secondary clinical outcomes, including 1-hour headache response; 2-hour pain-free response; absence of nausea, photophobia, and phonophobia; functional improvement; use of rescue medication; treatment acceptability; and sustained headache response (P <.05). Overall, treatment-related adverse events were low, nausea being the only adverse event with an incidence of 2% or higher (4.9% with eletriptan, 4.2% sumatriptan, 2.8% placebo).
This trial confirmed that eletriptan 40 mg offers superior efficacy in treating migraine pain and associated symptoms and in restoring patient functioning when compared with sumatriptan 100 mg.
确认40毫克依立曲坦相对于100毫克舒马曲坦的疗效优势。背景:在两项研究中,80毫克依立曲坦与50毫克和100毫克舒马曲坦相比,已显示出显著更高的疗效。在之前的一项试验中,40毫克依立曲坦显示出比100毫克舒马曲坦显著更高的疗效。
根据国际头痛协会标准诊断为偏头痛的2113例患者,采用双盲、双模拟、平行组设计进行随机分组,并用40毫克依立曲坦、100毫克舒马曲坦或安慰剂治疗单次偏头痛发作。主要终点是2小时头痛缓解情况。次要终点包括1小时头痛缓解率、无痛率、无相关症状、1小时和2小时的功能反应以及持续性头痛缓解情况。
给药后2小时,40毫克依立曲坦的头痛缓解率(67%)显著高于100毫克舒马曲坦(59%;P<.001)和安慰剂(26%;P<.0001)。在包括1小时头痛缓解、2小时无痛反应、无恶心、畏光和畏声、功能改善、使用急救药物、治疗可接受性以及持续性头痛缓解(P<.05)等次要临床结局方面,40毫克依立曲坦始终显示出比100毫克舒马曲坦有显著(P<.01)疗效。总体而言,与治疗相关的不良事件发生率较低,恶心是唯一发生率达到或高于2%的不良事件(依立曲坦为4.9%,舒马曲坦为4.2%,安慰剂为2.8%)。
该试验证实,与100毫克舒马曲坦相比,40毫克依立曲坦在治疗偏头痛疼痛及相关症状以及恢复患者功能方面具有卓越疗效。