Bendtsen L, Mattsson P, Zwart J-A, Lipton R B
Copenhagen Headache Research Centre, Department of Neurology, Glostrup Hospital, University of Copenhagen, Copenhagen, Denmark.
Cephalalgia. 2003 Sep;23(7):487-90. doi: 10.1046/j.1468-2982.2003.00528.x.
The objective was to assess the placebo response in randomized clinical trials of analgesics in the treatment of migraine attacks. We included placebo-controlled studies that used the criteria of the International Headache Society for the diagnosis of migraine and headache response as the primary efficacy parameter. In the 11 studies that qualified for inclusion, headache response occurred after placebo treatment in 7-50% of the migraineurs with an average placebo response rate of 30% (95% confidence interval (CI) 23-36). Two hours after treatment with placebo an average of 9% (95% CI 7-12, range 7-17%) of the patients were found to be pain free. In conclusion, the average headache response rate to placebo was 30% in randomized clinical trials of analgesics in migraine with a tremendous variation among studies. Placebo response rates vary with the choice of primary efficacy measure as well as patient characteristics and study design.
目的是评估镇痛药治疗偏头痛发作的随机临床试验中的安慰剂反应。我们纳入了安慰剂对照研究,这些研究采用国际头痛协会的标准诊断偏头痛,并将头痛反应作为主要疗效参数。在符合纳入标准的11项研究中,7%至50%的偏头痛患者在接受安慰剂治疗后出现头痛反应,平均安慰剂反应率为30%(95%置信区间[CI]23 - 36)。安慰剂治疗两小时后,平均有9%(95%CI 7 - 12,范围7 - 17%)的患者疼痛消失。总之,在偏头痛镇痛药随机临床试验中,安慰剂的平均头痛反应率为30%,各研究之间存在巨大差异。安慰剂反应率因主要疗效测量方法的选择以及患者特征和研究设计而异。