跳至主要内容
临床试验/NCT01768416
NCT01768416已完成不适用

Measuring Depth of Unconsciousness at the End of Life: the Reliability of the BIS Monitoring as an Assessment Tool Versus Sedation Scales

University Hospital, Ghent1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2013年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
10
试验地点
1
主要终点
Measuring the accuracy of BIS monitoring in assessing the evolution of the level of consciousness in pre-terminal patients

研究概览

简要总结

The purpose of this study is to use the BIS monitor to assess the degree of consciousness in pre-terminal palliative patients admitted to our palliative care unit and to ascertain if this tool provides a more accurate assessment of consciousness in this specific group of patients than clinical observation of consciousness and the use of sedation scales.

We hypothesize that the measured BIS results provide a more accurate assessment of the patient's level of consciousness than routine clinical observation or the use of sedation scales.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Pre-terminal palliative patients with a life expectancy of 72 hours or less at the start of the observation.

排除标准

  • lack of consent of patient or representative

结局指标

主要结局

Measuring the accuracy of BIS monitoring in assessing the evolution of the level of consciousness in pre-terminal patients

时间窗: 72 hours

Measuring the accuracy of BIS monitoring in assessing the evolution of the level of consciousness in pre-terminal patients with a life expectancy of 72 hours or less from the moment of the first clinical signs of dying and loss of consciousness until the moment of death.

次要结局

  • Determining the evolution of BIS values, measured in pre-terminal patients(72 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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