跳至主要内容
临床试验/NL-OMON46115
NL-OMON46115招募中不适用

Mobile Vital Sign tracking in high risk surgical ward patients - MoViSign

Ziekenhuisgroep Twente0 个研究点目标入组 80 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
招募中
发起方
入组人数
80

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 至 99(—)

入选标准

  • The study population includes two patient groups:
  • 1. Patients aged > 18 years undergoing elective oesophageal and gastric resection admitted to the gastrointestinal surgical ward for postoperative care
  • 2. Patients aged > 70 undergoing hip fracture surgery acutely admitted to the geriatric-trauma ward for pre- and postoperative care

排除标准

  • 1. Contraindications for use of vital sign sensor patch (i.e. skin allergy, implanted medical devices, contact isolation, etc.)
  • 2. Diagnosed or suspected delirium, cognitive impairment, or dementia

研究者

发起方
Ziekenhuisgroep Twente

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