跳至主要内容
临床试验/NL-OMON51127
NL-OMON51127尚未招募不适用

Clinical efficacy of continuous remote monitoring compared to intermittent monitoring on a surgical ward in a large European teaching hospital - Sensible trial

Albert Schweitzer Ziekenhuis0 个研究点目标入组 285 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
285

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

年龄范围
18 至 99(—)

入选标准

  • At least 18 years old; surgical, gastroenterology and gynaecological oncology
  • surgical admissions; expected length of stay > 24 h; informed consent

排除标准

  • An allergy to skin adhesives, wound or skin lesion near the application site,
  • patients with a pacemaker or implantable cardioverter defibrillator, patients
  • in a palliative trajectory, patients waiting for placement in a nursery home.

研究者

相似试验