跳至主要内容
临床试验/NL-OMON38784
NL-OMON38784已完成不适用

A Prospective, Nonrandomized, Noninvasive Study to Compare Nexfin CO-trek Cardiac Output with Trans-Thoracic Echo Cardiography Cardiac Output - TTE/Nexfin Clinical Study

Edwards Lifesciences LLC0 个研究点目标入组 120 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
已完成
入组人数
120

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

  • Potential Subjects must:
  • - be at least 18 years of age
  • - must give signed written informed consent

排除标准

  • Subjects will be excluded if any of these items exist:
  • 1. Aortic valve regurgitation
  • 2. Aortic stenosis or aneurysms
  • 3. History of uncontrolled cardiac arrhythmia
  • 4. Any peripheral vascular disease or conditions such as Raynaud*s disease or Buerger*s disease
  • 5. Insufficient perfusion of the digits
  • 6. Inability to place the finger cuff appropriately due to subject anatomy or condition
  • 7. Known pregnancy.

研究者

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