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临床试验/ISRCTN72502609
ISRCTN72502609已完成不适用

Computer-assisted ALerting and Monitoring System

Oxford BioSignals Ltd (UK)0 个研究点目标入组 400 人开始时间: 2005年6月10日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
400

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • Male or female patients, 18 years or older, undergoing 'high-risk' elective or emergency surgical procedures, or presenting with an acute medical problem of at least moderate severity.

排除标准

  • Those subject to additional protections; this includes pregnant women and persons with mental illness or disability, patients refusing consent, children (less than 18 years old), patients undergoing cardiac surgery, patients undergoing surgery for burns, patients undergoing surgery of the thoracic aorta, patients whose anatomy precludes the use of the required monitoring, patients expected to be sufficiently mobile to leave the bed space unaided within 72 hours of operation or recruitement.
  • Patients in the intensive care unit.

研究者

发起方
Oxford BioSignals Ltd (UK)

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