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氧化阿米替林治疗慢性紧张性头痛的有效性及耐受性——一项对比氧化阿米替林、阿米替林及安慰剂的多中心双盲研究

[Effectiveness and tolerance of amitriptyline oxide in chronic tension headache--a multicenter double-blind study versus amitriptyline versus placebo].

作者信息

Pfaffenrath V, Diener H C, Isler H, Meyer C, Scholz E, Taneri Z, Wessely P, Zaiser-Kaschel H, Haase W, Fischer W

机构信息

Neurologische Praxis, München.

出版信息

Nervenarzt. 1993 Feb;64(2):114-20.

PMID:8450893
Abstract

Tricyclic antidepressants, especially amitriptyline, are the medication of first choice in the treatment of chronic tension headache. Few previous studies meet modern standards of study design and statistical analysis. Tolerability and efficacy of 60-90 mg amitriptyline oxide (AO) as a single dose in the evening were compared with 50-75 mg amitriptyline (AM) and placebo (PL) in a double-blind, parallel-group trial consisting of a 4-week baseline phase and 12 weeks of treatment. The 3-armed study was conducted in 7 centers. The inclusion criterion was tension-type headache on at least 15 days monthly with a duration of at least 6 months. Exclusion criteria were a migraine history, previous participation in another clinical trial within the last 3 months, drug abuse, medication with other antidepressants or tranquilizers, current use of other acknowledged prophylactic headache medication, lack of compliance, major psychiatric disorder according to DSM-III and medical contra-indications against tricyclic antidepressants. The primary study endpoint was a reduction at least 50% of the product of headache duration and frequency and a reduction at least 50% in headache intensity. Statistics used were Fisher's Exact Test and an analysis of variance. A total of 211 patients were included in this trial. One hundred ninety-seven cases, 87 males and 110 females, with a mean age of 38 +/- 13 (18-68) years, could be analysed completely (66 AO, 67 AM, 64 PL). With regard to the strictly defined primary study endpoint, no significant difference emerged between AO, AM and PL: treatment responders were 30.3% with AO, 22.4% with AM and 21.9% with PL (PAO-PL = 0.3210, PAM-PL = 1.000, PAO-AM = 0.3299 respectively).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

三环类抗抑郁药,尤其是阿米替林,是治疗慢性紧张性头痛的首选药物。以往很少有研究符合现代研究设计和统计分析标准。在一项双盲、平行组试验中,比较了晚上单次服用60 - 90毫克氧化阿米替林(AO)与50 - 75毫克阿米替林(AM)及安慰剂(PL)的耐受性和疗效,该试验包括4周的基线期和12周的治疗期。这项三臂研究在7个中心进行。纳入标准为每月至少15天出现紧张型头痛且持续时间至少6个月。排除标准包括偏头痛病史、过去3个月内曾参与另一项临床试验、药物滥用、使用其他抗抑郁药或镇静剂、目前正在使用其他公认的预防性头痛药物、依从性差、符合《精神疾病诊断与统计手册第三版》(DSM - III)的重度精神障碍以及三环类抗抑郁药的医学禁忌证。主要研究终点是头痛持续时间与频率的乘积至少降低50%以及头痛强度至少降低50%。使用的统计方法是Fisher精确检验和方差分析。本试验共纳入211例患者。其中197例(87例男性和110例女性),平均年龄38±13(18 - 68)岁,能够进行完整分析(66例AO组、67例AM组、64例PL组)。关于严格定义的主要研究终点,AO组、AM组和PL组之间未出现显著差异:AO组治疗有效率为30.3%,AM组为22.4%,PL组为21.9%(PAO - PL = 0.3210,PAM - PL = 1.000,PAO - AM = 0.3299)。(摘要截选至250字)

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