跳至主要内容
临床试验/NL-OMON21083
NL-OMON21083已完成不适用

Randomized trial comparing the effects of BIS monitoring and daily wake up with clinical assessment on ICU length of stay and costs in sedated ICU patients.

Academisch Medisch Centrum Amsterdam0 个研究点目标入组 600 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
入组人数
600

研究概览

简要总结

/A

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. Consecutive ICU patients who are 18 years or older;
  • 2. Patients who are sedated for less than 24 hours;

排除标准

  • 1. Patients who have been transferred from another ICU where sedative agents have been administered for more than 24 hours;
  • 2. Patients with a decreased level of consciousness (defined as a Glasgow Coma Scale score of 12 or lower immediately before sedatives were administrated), will also be excluded;

研究者

发起方
Academisch Medisch Centrum Amsterdam

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