跳至主要内容
临床试验/KCT0008487
KCT0008487尚未招募Unknown

Accuracy evaluation of non-invasive hemodynamic monitor HemoVistaTM (BiLab Co. Ltd. Korea) in the critically ill patients: A prospective observational study

Asan Medical Center0 个研究点目标入组 20 人开始时间: 待定最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
入组人数
20

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
20(Year) 至 o Limit(—)
性别
All

入选标准

  • Adult patients aged 20 or older admitted to the surgical intensive care unit of Asan Medical Center in Seoul, who using arterial catheter cardiac output monitoring device at the time of participation.

排除标准

  • Clinically significant arrhythmia (e.g., atrial fibrillation) that may affect the calculation of stroke volume
  • Patients with cardiac pacemakers or defibrillators
  • Patients with mechanical circulation aids, such as an extracorporeal oxygen supply (VA-ECMO) or an aortic balloon pump (IABP)
  • Patients with trauma or skin lesions in the HemoVistaTM sensor attachment (anterior chest)
  • Any other person deemed inappropriate by researchers

研究者

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