跳至主要内容
临床试验/NL-OMON52930
NL-OMON52930招募中不适用

Prediction of Post-induction Hypotension with Arterial Pulse wave applied Machine Learning, a non-randomized prospective data collection observational study. - PREP trial

Academisch Medisch Centrum0 个研究点目标入组 1,200 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
入组人数
1,200

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

  • Elective surgical patients:
  • - >=18 years of age
  • - Informed consent
  • - Planned for any type of elective surgery
  • Intensive Care Unit patients requiring intubation:
  • - >= 18 years of age
  • - Informed consent or deferred consent
  • - Requiring (emergency) intubation
  • Intensive Care Unit patients requiring elective tracheostomy:
  • - >= 18 years of age
  • - Informed consent or deferred consent
  • - Requiring elective tracheostomy

排除标准

  • Elective surgical patients:
  • - Any right-sided structural pathology or reduced cardiac function (Tapse
  • <1.5cm) (only phase 2)
  • - Severe cardiac arrhythmias (with high heart rate), including atrial
  • fibrillation
  • - Abnormal anatomy of the fingers
  • - Emergency surgery (only phase 2)
  • - Allergy for medication used in study protocol
  • - Subjects will be excluded if both noninvasive blood pressure (with the finger
  • cuff) and invasive blood pressure (with an arterial cannula already available
  • due to standard of care) cannot be measured according to the Instructions for
  • Use of the CS/EV1000/HemoSphere system.
  • Intensive Care Unit patients requiring intubation:
  • - Subjects will be excluded if both noninvasive blood pressure (with the finger
  • cuff) and invasive blood pressure (with an arterial cannula already available
  • due to standard of care) cannot be measured according to the Instructions for
  • Use of the CS/EV1000/HemoSphere system.
  • Intensive Care Unit patients requiring elective tracheostomy:
  • - Subjects will be excluded if both noninvasive blood pressure (with the finger
  • cuff) and invasive blood pressure (with an arterial cannula already available
  • due to standard of care) cannot be measured according to the Instructions for
  • Use of the CS/EV1000/HemoSphere system.

研究者

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