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首页> 外文期刊>Journal of clinical psychopharmacology >A generalized estimating equation approach to analysis of maintenance of wakefulness testing in a study of lisdexamfetamine dimesylate, armodafinil, and placebo in sleep-deprived adults
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A generalized estimating equation approach to analysis of maintenance of wakefulness testing in a study of lisdexamfetamine dimesylate, armodafinil, and placebo in sleep-deprived adults

机译:赖斯氨苯丙胺二甲磺酸盐,阿莫达非尼和安慰剂用于睡眠剥夺成人的研究中,用于清醒测试维持分析的广义估计方程法

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摘要

In a study of acute sleep deprivation in healthy male volunteers randomized to double-blind treatment with lisdexamfetamine dimesylate (20, 50, or 70 mg), placebo control, or an active control (armodafinil 250 mg), Maintenance of Wakefulness Test data were compared using a generalized estimating equation analysis to eliminate the need for unequivocal sleep latency imputation. Compared with placebo across all Maintenance of Wakefulness Tests, all active treatments were associated with lower risk of falling asleep (risk ratio [95% confidence interval]): 0.45 (0.27-0.76; P = 0.0026), 0.10 (0.05-0.20; P < 0.0001), and 0.05 (0.02-0.14; P < 0.0001) for 20, 50, and 70 mg lisdexamfetamine dimesylate, respectively, and 0.11 (0.06-0.21; P < 0.0001) for the active control. Sleep-risk ratios were similar for lisdexamfetamine dimesylate 50 or 70 mg and for the active control, but lisdexamfetamine 20 mg was associated with a greater risk of falling asleep compared with the active control (4.13 [1.97-8.67]; P = 0.0002). Generalized estimating equation analysis detected wake-promoting effects of active treatments and eliminating data imputation, suggesting model utility in future studies.
机译:在一项针对健康男性志愿者的急性睡眠剥夺的研究中,随机分配接受来塞米特胺二甲磺酸盐(20、50或70 mg),安慰剂对照或有效对照(阿莫达非尼250 mg)的双盲治疗,比较了维持清醒测试的数据使用广义估计方程分析来消除对明确的睡眠潜伏期估算的需要。与所有维持清醒测试的安慰剂相比,所有积极治疗与入睡的风险更低(风险比[95%置信区间]):0.45(0.27-0.76; P = 0.0026),0.10(0.05-0.20; P分别为20 mg,50 mg和70 mg的dexdexamfetamine dimesylate的<0.0001)和0.05(0.02-0.14; P <0.0001),对于活性对照组为0.11(0.06-0.21; P <0.0001)。来塞米特50或70 mg的二甲磺酸赖氨酸和活性对照组的睡眠风险比相似,但赖塞米特20 mg的入睡风险比活性对照组更高(4.13 [1.97-8.67]; P = 0.0002)。广义估计方程分析检测到积极治疗的促醒作用并消除了数据归因,这表明该模型在未来的研究中具有实用性。

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