Sargent J, Kirchner J R, Davis R, Kirkhart B
Menninger Clinic, Topeka, KS 66601, USA.
Neurology. 1995 Aug;45(8 Suppl 7):S10-4.
The efficacy and tolerability of oral sumatriptan (Imitrex tablets) were assessed in 187 migraineurs enrolled in a randomized, double-blind, parallel-group, placebo-controlled study. In the clinic, patients received oral sumatriptan 25 mg, 50 mg, or 100 mg, or placebo, for the treatment of a migraine attack. The results demonstrate that by 2 hours postdose, 52 to 57% of patients treated with sumatriptan 25 mg, 50 mg, 100 mg compared with 17% of patients treated with placebo achieved relief of headache (p < 0.05 for each sumatriptan group vs placebo). By 4 hours postdose, 65 to 78% of sumatriptan-treated patients compared with 19% of placebo-treated patients achieved relief of headache (p < 0.05 for each sumatriptan group vs placebo). Oral sumatriptan also effectively relieved nausea and photophobia and improved clinical disability. No serious or unusual adverse events were reported, and the pattern and incidence of adverse events did not vary among the sumatriptan doses. Each dose--25 mg, 50 mg, or 100 mg--of sumatriptan was effective and generally well tolerated.
在一项随机、双盲、平行组、安慰剂对照研究中,对187名偏头痛患者评估了口服舒马曲坦(依米曲坦片)的疗效和耐受性。在诊所中,患者接受25毫克、50毫克或100毫克口服舒马曲坦或安慰剂治疗偏头痛发作。结果表明,给药后2小时,接受25毫克、50毫克、100毫克舒马曲坦治疗的患者中,52%至57%的患者头痛得到缓解,而接受安慰剂治疗的患者中这一比例为17%(各舒马曲坦组与安慰剂组相比,p<0.05)。给药后4小时,舒马曲坦治疗的患者中有65%至78%头痛得到缓解,而安慰剂治疗的患者中这一比例为19%(各舒马曲坦组与安慰剂组相比,p<0.05)。口服舒马曲坦还能有效缓解恶心和畏光症状,并改善临床失能情况。未报告严重或异常不良事件,且不良事件的类型和发生率在舒马曲坦各剂量组之间无差异。舒马曲坦的每个剂量——25毫克、50毫克或100毫克——均有效且一般耐受性良好。