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临床试验/ACTRN12623001318673
ACTRN12623001318673尚未招募Unknown

Automated vital sign monitoring devices in acutely unwell general medical inpatients: an exploratory study

Fisher & Paykel Healthcare Limited0 个研究点目标入组 27 人开始时间: 2023年12月15日最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
入组人数
27

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

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Patients admitted under a medical team <24 hours
  • Anticipated to remain an inpatient in Wellington hospital for >24 hours
  • EWS =/> 4 at time of eligibility assessment

排除标准

  • Planned surgical intervention requiring transfer to an operating theatre within 24 hours
  • Cardiac pacemaker
  • Primarily receiving end of life care (Goals of Care D)
  • HDB/ICU admissions
  • Invasive/non-invasive ventilation
  • Imminent need for ICU admission (currently planning for ICU admission)
  • Meeting MET call criteria at eligibility assessment (EWS =/>10 or any parameter in ‘blue zone’)
  • Practical reasons that a chest wall sensing device cannot be applied (MRI scanner, skin disease, dressings, etc.)
  • Cognitive impairment or impaired consciousness precluding informed consent and ability to co-operate with application of continuous monitoring devices
  • Pregnancy or breastfeeding

研究者

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