Sandrini G, Franchini S, Lanfranchi S, Granella F, Manzoni G C, Nappi G
IRCCS C. Mondino Foundation, University Center for Headache and Adaptive Disorders, Pavia I Unit, Italy.
Int J Clin Pharmacol Res. 1998;18(3):145-50.
The purpose of this study was to evaluate the effectiveness of a new formulation of ibuprofen (ibuprofen-arginine [IA]) in the treatment of migraine attacks. This is a faster absorbed formulation as compared with ibuprofen alone. The rapidity of action is considered to be a crucial factor in the treatment of migraine attacks. Forty migraine patients participated in this multicenter, double-blind, crossover, randomized, placebo-controlled trial. Each patient was treated with a single oral dose of IA 400 mg or placebo during two consecutive migraine attacks. The results confirm the efficacy of IA, with a significant (p < 0.05) improvement in pain relief at 30 min after treatment. A statistically significant (p < 0.001) reduction in pain intensity was observed at 1, 2, 4 and 6 h after treatment with ibuprofen as compared with placebo. IA was well tolerated and our data indicate that this new formulation of ibuprofen is valuable in the treatment of acute migraine attacks.
本研究的目的是评估布洛芬的一种新制剂(布洛芬精氨酸[IA])治疗偏头痛发作的有效性。与单独使用布洛芬相比,这是一种吸收更快的制剂。作用速度被认为是治疗偏头痛发作的关键因素。40名偏头痛患者参与了这项多中心、双盲、交叉、随机、安慰剂对照试验。每位患者在连续两次偏头痛发作期间接受单次口服400毫克IA或安慰剂治疗。结果证实了IA的疗效,治疗后30分钟疼痛缓解有显著改善(p<0.05)。与安慰剂相比,布洛芬治疗后1、2、4和6小时疼痛强度有统计学显著降低(p<0.001)。IA耐受性良好,我们的数据表明,这种布洛芬新制剂在治疗急性偏头痛发作方面具有价值。