首页> 外文期刊>Cephalalgia >A multicentre, double-blind, randomized, placebo-controlled, parallel group study of multiple treatments of botulinum toxin type A (BoNTA) for the prophylaxis of episodic migraine headaches.
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A multicentre, double-blind, randomized, placebo-controlled, parallel group study of multiple treatments of botulinum toxin type A (BoNTA) for the prophylaxis of episodic migraine headaches.

机译:一项多中心,双盲,随机,安慰剂对照,平行分组研究,涉及多种治疗A型肉毒杆菌毒素(BoNTA)的预防偏头痛的方法。

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摘要

Our aim was to evaluate the safety and efficacy of botulinum toxin type A (BoNTA; BOTOX) for prophylaxis of episodic migraine. In this double-blind, placebo-controlled study, patients were randomized to 225, 150 or 75 U of BoNTA or placebo after a 30-day placebo run-in for three 90-day treatment cycles. The primary efficacy end-point was the mean reduction from baseline in the frequency of migraine episodes at day 180 in the placebo non-responder stratum. All groups (N = 495) improved, with no significant differences. At day 180, the frequency of migraine episodes was reduced from baseline means of 4.3, 4.7, 4.7 and 4.4 by 1.6, 1.7, 1.5 and 1.4 for BoNTA 225 U, 150 U and 75 U and placebo, respectively. The primary end-point was not met. Treatment-related adverse events were transient and mild to moderate. BoNTA treatment was safe and well tolerated but did not result in significantly greater improvement than placebo in this study. Several factors may have confounded the results.
机译:我们的目标是评估A型肉毒杆菌毒素(BONTA; BOTOX)预防发作性偏头痛的安全性和有效性。在这项双盲,安慰剂对照研究中,将患者在30天的安慰剂磨合后连续三个90天的治疗周期,随机分配到225、150或75 U的BoNTA或安慰剂中。主要功效终点是安慰剂无反应层中第180天偏头痛发作频率相对于基线的平均降低。所有组(N = 495)均改善,无显着差异。在第180天,偏头痛发作的频率分别比BoNTA 225 U,150 U和75 U和安慰剂的基线平均值4.3、4.7、4.7和4.4分别降低了1.6、1.7、1.5和1.4。主要终点未达到。与治疗相关的不良事件是短暂的,轻度至中度。在这项研究中,BoNTA治疗是安全且耐受良好的,但没有比安慰剂产生明显更大的改善。几个因素可能使结果混淆。

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