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可乐定预防性治疗偏头痛。一项对照临床试验。

Prophylactic treatment of migraine with clonidine. A controlled clinical trial.

作者信息

Mondrup K, Moller C E

出版信息

Acta Neurol Scand. 1977 Nov;56(5):405-12. doi: 10.1111/j.1600-0404.1977.tb01448.x.

Abstract

In a double-blind crossover trial of two 12-week treatment periods with a 4-week treatment free interval, to which 21 patients were admitted, there was no statistically significant difference between clonidine 75 microgram twice daily and placebo in the total number of headache days, migraine indices, duration of attacks, number of severe attacks and consumption of acute attack treatment. However, there was a marked reduction in number of headache days, migraine indices, duration of attacks and consumption of acute attack treatment during the second treatment period compared to the first treatment period, regardless of the treatment regime. This was presumably a result of prolonged treatment and frequent attention and not an effect of the active drug. 32 patients entered the trial, but 11 dropped out. Of the 21 patients completing the trial, 16 were women; the median age was 34 years (range 17-54 years) and the median duration of headaches 12 years (range 1-40 years). Only mild side-effects were registered and no laboratory abnormalities were seen.

摘要

在一项双盲交叉试验中,有两个为期12周的治疗期,中间有4周的无治疗间隔期,共有21名患者参与。在每日两次服用75微克可乐定与服用安慰剂之间,头痛天数、偏头痛指数、发作持续时间、严重发作次数以及急性发作治疗药物的使用总量方面,均无统计学上的显著差异。然而,与第一个治疗期相比,第二个治疗期的头痛天数、偏头痛指数、发作持续时间以及急性发作治疗药物的使用量均有显著减少,且与治疗方案无关。这可能是长期治疗和频繁关注的结果,而非活性药物的作用。32名患者进入试验,但11名退出。在完成试验的21名患者中,16名是女性;年龄中位数为34岁(范围17 - 54岁),头痛持续时间中位数为12年(范围1 - 40年)。仅记录到轻微的副作用,未发现实验室异常。

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