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首页> 外文期刊>Current medical research and opinion >A comparative, randomised, double-blind study of trazodone prolonged-release and paroxetine in the treatment of patients with major depressive disorder.
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A comparative, randomised, double-blind study of trazodone prolonged-release and paroxetine in the treatment of patients with major depressive disorder.

机译:曲唑酮缓释和帕罗西汀在治疗重度抑郁症患者中的比较,随机,双盲研究。

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OBJECTIVES: To evaluate the efficacy and safety of trazodone prolonged release compared with paroxetine in the treatment of patients with major depression.Research design and methods: A total of 108 patients aged 20-68 years were enrolled in this multicentre, double-blind, double-dummy, randomised, paroxetine-controlled study. Each patient received 3 days single-blind placebo treatment followed by 6 weeks double-blind treatment with either trazodone prolonged release 150-450 mg/day (n = 55) or paroxetine 20-40 mg/day (n = 53).OUTCOME MEASURES: Efficacy was evaluated by the rate of patients responding to each treatment and considered to be in remission, and by mean changes from baseline in the Hamilton Depression Rating scale scores (HAM-D), Montgomery Asberg Depression Rating Scale scores (MADRS), and Clinical Global Impression (CGI) - Severity and Global Improvement scores. Time to onset of efficacy and safety were assessed.RESULTS: Trazodone and paroxetine were equally effective at reducing symptoms of depression and promoting remission. Onset of efficacy was slightly faster for patients treated with paroxetine. Overall, there were no significant differences between the groups at endpoint in efficacy measures, and in percentage of responders (> 85%) or patients in remission (> 65%). Sleep disorders (HAM-D subset) were significantly less evident for patients in the trazodone group at the end of the study (p < 0.05). Adverse drug reactions were reported by 35% of trazodone-treated patients (mainly of the nervous system) and 26% of paroxetine-treated patients (mainly gastrointestinal), although none was considered to be serious.CONCLUSIONS: This study showed that after a 6-week period trazodone and paroxetine are not different in reducing the symptoms of depression and, in many patients, in producing the remission of the illness. The known divergence in tolerability profile of the two medications, related to their differing pharmacological properties, was also confirmed. Trazodone may be of advantage in depressed patients with sleep difficulties.
机译:目的:评价曲唑酮缓释片与帕罗西汀相比在重度抑郁症患者中的疗效和安全性。研究设计和方法:本研究共纳入108名20-68岁的患者,采用双盲,双盲,双盲治疗。 -虚拟,随机,帕罗西汀对照研究。每位患者接受3天的单盲安慰剂治疗,然后进行6周的双盲治疗,曲唑酮延长释放150-450 mg /天(n = 55)或帕罗西汀20-40 mg /天(n = 53)。 :通过对每种治疗有反应且被认为处于缓解状态的患者比率以及汉密尔顿抑郁量表评分(HAM-D),蒙哥马利阿斯伯格抑郁量表评分(MADRS)与基线相比的平均变化来评估疗效临床总体印象(CGI)-严重程度和总体改善得分。结果:曲唑酮和帕罗西汀在减轻抑郁症状和促进缓解方面同样有效。帕罗西汀治疗的患者起效略快。总体而言,两组在疗效指标,反应者百分比(> 85%)或缓解患者(> 65%)方面在终点之间无显着差异。在研究结束时,曲唑酮组患者的睡眠障碍(HAM-D子集)明显较少(p <0.05)。据报告,曲唑酮治疗的患者(主要是神经系统)有35%的药物不良反应,帕罗西汀治疗的患者(主要是胃肠道)有26%的药物不良反应。结论:该研究表明6一周内曲唑酮和帕罗西汀在减轻抑郁症状以及许多患者减轻疾病症状方面没有不同。还证实了与两种药物的不同药理特性有关的两种药物的耐受性差异。曲唑酮对睡眠困难的抑郁症患者可能有利。

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