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An assessment of the efficacy and safety of eszopiclone in the treatment of transient insomnia in healthy adults.

机译:在健康成人中,依佐匹克隆治疗短暂性失眠的疗效和安全性评估。

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BACKGROUND AND PURPOSE: This randomized, double-blind, placebo-controlled study assessed the efficacy and safety of eszopiclone, a non-benzodiazepine hypnotic agent, in healthy adults using the first-night effect model of transient insomnia. PATIENTS AND METHODS: A total of 436 healthy, normal sleeping participants were randomized to receive either eszopiclone 1, 2, 3, or 3.5mg, or placebo. Efficacy and next-morning effects were evaluated via polysomnography (PSG), Digit Symbol Substitution Test (DSST), and self-report. RESULTS: Patients treated with eszopiclone had significantly less PSG latency to persistent sleep (all doses except 1mg; P
机译:背景与目的:这项随机,双盲,安慰剂对照的研究使用短暂性失眠的第一夜效应模型评估了非苯二氮杂类催眠药埃索比克隆的功效和安全性。患者与方法:共有436名健康,正常睡眠的参与者被随机分配接受eszopiclone 1、2、3或3.5mg或安慰剂。通过多导睡眠图(PSG),数字符号替代测试(DSST)和自我报告来评估疗效和下次早晨的效果。结果:依佐匹克隆治疗的患者持续睡眠的PSG潜伏期(除1mg以外的所有剂量; P

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