跳至主要内容
临床试验/CTRI/2018/02/011713
CTRI/2018/02/011713进行中(未招募)3 期

Pilot study on using a purpose built device (PreSense) to improve turn-protocol compliance

Healthcare Technology Innovation Centre0 个研究点目标入组 40 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
进行中(未招募)
入组人数
40

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

入选标准

  • All adults admitted to Intensive Care Unit (ICU) who are considered at risk of acquiring
  • pressure ulcers can be enrolled in the study.

排除标准

  • 1. Patients who cannot have the wearable device attached to their chest.
  • 2. Patients who currently have implantable cardiovascular- defibrillator or pacemaker.

研究者

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