Bomhof M, Paz J, Legg N, Allen C, Vandormael K, Patel K
Ignatius Ziekenhuis, Breda, The Netherlands.
Eur Neurol. 1999;42(3):173-9. doi: 10.1159/000008094.
Rizatriptan (MAXALT(TM), Merck & Co., Inc.) is a selective 5-HT(1B/1D) receptor agonist with rapid oral absorption and early onset of action for the acute treatment of migraine. This randomized, double-masked, double-dummy, placebo-controlled study compared rizatriptan 10 mg to naratriptan (NARAMIG(TM), AMERGE(TM), both Glaxo Wellcome plc) 2.5 mg in 522 patients treating a single migraine attack. Rizatriptan was more effective than naratriptan. Rizatriptan provided earlier headache relief than naratriptan (hazard ratio 1.62, p < 0.001), acting as early as 30 min. More patients were pain free at 2 h on rizatriptan than on naratriptan (44.8 vs. 20.7%, p < 0.001). Rizatriptan also provided earlier relief of associated migraine symptoms within 2 h than naratriptan and more patients had normal function at 2 h (39.3 vs. 22.6%, p < 0. 001). Both active treatments were effective compared to placebo. Both active treatments were well tolerated. The most common side effects with rizatriptan were dizziness, asthenia/fatigue, nausea and somnolence, while the most common side effects with naratriptan were dizziness and asthenia/fatigue.
利扎曲普坦(MAXALT™,默克公司)是一种选择性5-HT(1B/1D)受体激动剂,口服吸收迅速,起效早,用于偏头痛的急性治疗。这项随机、双盲、双模拟、安慰剂对照研究在522例治疗单次偏头痛发作的患者中,将10 mg利扎曲普坦与2.5 mg那拉曲普坦(NARAMIG™,AMERGE™,均为葛兰素威康公司)进行了比较。利扎曲普坦比那拉曲普坦更有效。利扎曲普坦比那拉曲普坦能更早缓解头痛(风险比1.62,p<0.001),最早在30分钟起效。服用利扎曲普坦2小时时无痛的患者比服用那拉曲普坦的患者更多(44.8%对20.7%,p<0.001)。利扎曲普坦在2小时内也比那拉曲普坦更早缓解相关偏头痛症状,且2小时时有更多患者功能正常(39.3%对22.6%,p<0.001)。与安慰剂相比,两种活性治疗均有效。两种活性治疗耐受性良好。利扎曲普坦最常见的副作用是头晕、乏力/疲劳、恶心和嗜睡,而那拉曲普坦最常见的副作用是头晕和乏力/疲劳。