Guidotti M, Zanasi S, Garagiola U
Headache and Migraine Ambulatory, Sanrocco Centre, Como, Italy.
J Int Med Res. 1989 Jan-Feb;17(1):48-54. doi: 10.1177/030006058901700107.
A double-blind, within patient, randomized study to compare the efficacy and tolerability of acute rectal administration of 600 mg pirprofen capsules with matched placebo was carried out in 40 out-patients. They were divided into two groups of 20 patients each according to diagnosis of episodic headache or common or classic migraine. Treatment was given once during each of two consecutive attacks according to a crossover design. None of the patients was withdrawn after randomization. There was a statistically significant difference in favour of pirprofen as regards the preferences expressed by patients at the end of the trial: 34 patients preferred pirprofen, two preferred placebo and four patients had no preference. Pirprofen significantly reduced the duration of headache attack and associated symptoms, but not the peak of pain intensity. Tolerability of the drug was good.
一项双盲、患者自身随机对照研究在40名门诊患者中开展,比较600毫克吡洛芬胶囊直肠急性给药与匹配安慰剂的疗效和耐受性。根据发作性头痛或普通型或典型偏头痛的诊断,将他们分为两组,每组20名患者。按照交叉设计,在连续两次发作期间各给药一次。随机分组后没有患者退出研究。在试验结束时患者表达的偏好方面,吡洛芬具有统计学显著优势:34名患者更喜欢吡洛芬,2名更喜欢安慰剂,4名患者无偏好。吡洛芬显著缩短了头痛发作及相关症状的持续时间,但未降低疼痛强度峰值。该药物耐受性良好。