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Sublingual zolpidem is more effective than oral zolpidem in initiating early onset of sleep in the post-nap model of transient insomnia: a polysomnographic study.

机译:一项多导睡眠图研究显示,舌下唑吡坦比口服唑吡坦在启动小睡后失眠模型中的早起睡眠起效要好于口服唑吡坦。

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OBJECTIVE: OX22 is zolpidem formulated for sublingual administration. The primary objective of the present study was to evaluate the efficacy of single doses of sublingual zolpidem (5 and 10mg) versus oral zolpidem (10mg), with regard to latency to persistent sleep (LPS), in a post-nap model of insomnia. METHODS: Twenty-one healthy volunteers included in this study were recorded by polysomnography during 2 consecutive nights and, on the day in between, during a 2h nap. Eighteen out of these 21 subjects were finally analyzed. Treatment was randomly administered before the second recording night to subjects demonstrating at least 30min of sleep during the nap recording. RESULTS: Contrast analyses show that 10mg OX22 significantly shortened LPS compared to oral zolpidem administration of 10mg (12.8+/-9.9 and 18.4+/-11.3min, respectively; p<.05). No treatment effects could be evidenced on total sleep time, time awake after sleep onset and sleep architecture parameters for OX22 compared to oral zolpidem. All treatments were well tolerated and did not induce next-day residual effects. CONCLUSION: The present results show that OX22, a sublingual formulation of zolpidem, has a significant earlier sleep initiation as compared to an equivalent dose of oral zolpidem in healthy volunteers in a post-nap model of insomnia.
机译:目的:OX22是唑吡坦,用于舌下给药。本研究的主要目的是在失眠的小睡后模型中评估单剂量舌下含唑吡坦(5和10mg)与口服唑吡坦(10mg)相对于持续睡眠潜伏期(LPS)的疗效。方法:本研究中包括的21名健康志愿者在连续2个晚上以及午间2小时的午间通过多导睡眠监测仪进行记录。最后,对这21名受试者中的18名进行了分析。在第二个记录之夜之前,对显示出午睡记录期间至少睡眠30分钟的受试者进行随机治疗。结果:对比分析显示,与口服唑吡坦10mg相比,10mg OX22显着缩短LPS(分别为12.8 +/- 9.9和18.4 +/- 11.3min; p <.05)。与口服唑吡坦相比,OX22的总睡眠时间,睡眠开始后的清醒时间和睡眠结构参数均无治疗效果。所有治疗均耐受良好,不会引起第二天的残留效应。结论:目前的结果表明,与失眠后小睡的健康志愿者等效剂量的口服唑吡坦相比,唑吡坦的舌下制剂OX22具有显着的早期睡眠启动。

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