Gerber W D, Schellenberg R, Thom M, Haufe C, Bölsche F, Wedekind W, Niederberger U, Soyka D
Department of Medical Psychology, University of Kiel, Germany.
Funct Neurol. 1995 Jan-Feb;10(1):27-35.
The aim of the present study was to ascertain the comparative efficacy of cyclandelate, a migraine prophylactic with calcium overload blocking properties, versus propranolol, a non-selective beta-adrenergic blocker, and placebo. Based on different statistical analysis procedures (including time series analysis) a responder and nonresponder evaluation for cyclandelate and propranolol was performed. In addition, an attempt was made to identify the dose relationship of the various drugs on headache parameters. In a double-blind placebo-controlled study 84 patients were treated in a placebo run-in phase (4 weeks). The patients were then randomized by the statistical criterion of placebo responder and nonresponder to either the cyclandelate or the propranolol group. The total treatment period included a low-dosage phase (8 weeks) and high-dosage phase (8 weeks). All patients kept a headache diary before, during and after treatment. The data were assessed by time series analysis (ARIMA), as well as by analysis of variance and nonparametric statistics. Based on ARIMA statistics, 39.3% of the patients showed a significant improvement of migraine during treatment with cyclandelate compared with 29.4% placed on propranolol. Higher doses of cyclandelate and propranolol were more effective. Using the qualitative response-criterion of a 50% reduction in migraine symptoms, cyclandelate showed a response in 67.9% and propranolol in 41.2% of all cases. It can therefore be concluded that cyclandelate as well as propranolol are two comparable substances in the prophylactic treatment of migraine, with cyclandelate showing fewer side effects.
本研究的目的是确定具有钙超载阻断特性的偏头痛预防性药物环扁桃酯与非选择性β-肾上腺素能阻滞剂普萘洛尔及安慰剂相比的疗效。基于不同的统计分析程序(包括时间序列分析),对环扁桃酯和普萘洛尔进行了反应者与无反应者评估。此外,还试图确定各种药物在头痛参数方面的剂量关系。在一项双盲安慰剂对照研究中,84名患者在安慰剂导入期(4周)接受治疗。然后根据安慰剂反应者和无反应者的统计标准将患者随机分为环扁桃酯组或普萘洛尔组。总治疗期包括低剂量阶段(8周)和高剂量阶段(8周)。所有患者在治疗前、治疗期间和治疗后都记录头痛日记。数据通过时间序列分析(ARIMA)以及方差分析和非参数统计进行评估。基于ARIMA统计,与接受普萘洛尔治疗的29.4%患者相比,39.3%接受环扁桃酯治疗的患者偏头痛有显著改善。环扁桃酯和普萘洛尔的高剂量更有效。使用偏头痛症状减轻50%的定性反应标准,环扁桃酯在所有病例中的反应率为67.9%,普萘洛尔为41.2%。因此可以得出结论,环扁桃酯和普萘洛尔在偏头痛预防性治疗中是两种相当的药物,且环扁桃酯的副作用较少。