跳至主要内容
临床试验/NL-OMON50879
NL-OMON50879已完成不适用

Supporting early recognition of clinical deterioration for Mobile Vital signs monitoring of high-risk surgical patients - MoViSupport

Ziekenhuisgroep Twente0 个研究点目标入组 80 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
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 and older) undergoing elective surgery for resection
  • of malignant
  • tumors of the upper gastrointestinal tract (upper GI patients)
  • 2. Patients aged (70 years and older) undergoing surgery for a hip fracture and
  • admitted to the
  • hospital for pre- or postoperative care (hip fracture patients)

排除标准

  • 1. Contraindications for use of vital sign sensor patch (i.e. skin allergy,
  • implanted medical devices)
  • 2. Contact isolation

研究者

发起方
Ziekenhuisgroep Twente

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