跳至主要内容
临床试验/NL-OMON43659
NL-OMON43659已完成不适用

Sleep and biorhythm in ICU patients: a pilot study - Sleep and biorhythm in the IC

Philips0 个研究点目标入组 70 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Philips
入组人数
70

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • ICU patients
  • > 18 years of age
  • Expected stay in the ICU 48h or longer
  • Capable of understanding and speaking Dutch
  • Richmond agitation and sedation scale (RASS) * -3

排除标准

  • Pre-existing history or treatment of sleep pathology, severe visual or hearing impairment, alcohol addiction or illicit drug abuse
  • History of cognitive dysfunction (defined as dementia, traumatic brain injury, stroke or hepatic encephalopathy)
  • Previously discharged from the ICU during this hospital admission
  • Admission following neurosurgery (since underlying pathology, or the surgery itself, may interfere with sleep and cognitive function)

研究者

发起方
Philips

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