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临床试验/JPRN-UMIN000005591
JPRN-UMIN000005591已完成未知

Prediction and prevention of delirium - Prediction and prevention of delirium

Juntendo University Nerima Hospital0 个研究点目标入组 168 人开始时间: 2011年5月12日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
168

研究概览

简要总结

Results: Ramelteon was associated with lower risk of delirium (3% vs. 32%, P=.003), with a relative risk of 0.09 (95% confidence interval (CI), 0.01-0.69). Even after controlling for risk factors, ramelteon was still associated with a lower incidence of delirium (P=.01; odds ratio, 0.07; 95%CI, 0.008-0.54). Kaplan-Meier estimates of time to development of delirium were 6.94 days (95%CI, 6.82-7.06 days) for ramelteon and 5.74 days (5.05-6.42 days) for placebo. Comparison by log-rank test showed that the frequency of developing delirium was significantly lower in patients taking ramelteon than in those taking placebo (X2=9.83, P=.002). Conclusions and Relevance: Ramelteon administered nightly to elderly patients admitted for acute care may provide protection against delirium. This finding supports a possible pathogenic role of melatonin neurotransmission in delirium.

研究设计

研究类型
Interventional

入排标准

年龄范围
65years-old 至 90years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Severe liver dysfunction 2) Patients given fluvoxamine 3) Alcohol dependence, amphetamine abuse

研究者

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