ACTRN12623001193662尚未招募Unknown
Evaluation of the Accuracy of a Novel Sleep Monitoring Technology Compared to Polysomnography in the Intensive Care Unit
适应症
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 入组人数
- 33
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Diagnosis
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Aged 18 years and over
- •Expected ICU length of stay > 24 hours
- •Richmond Agitation Scale Score (RASS) between -2 to 0
- •- RASS score should be stable within these limits for the 2 hours preceding enrolment.
- •- Any divergence outside these parameters occurring between enrolment and application of the study devices should be discussed with the principal investigator to determine suitability to proceed.
排除标准
- •Suspected or confirmed diagnosis of acute central nervous system pathology
- •Acute head and neck injury or surgery
- •Acute psychiatric or behavioural disturbance
- •Acute toxic ingestion
- •History of seizures
- •Continuous infusions of propofol or benzodiazepines
- •Position restrictions that may limit the application of monitoring devices
- •The treating Intensivist’s perception that devices will be poorly tolerated by the patient for the study period
- •Previous enrolment in this study
研究者
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