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临床试验/ISRCTN91147138
ISRCTN91147138已完成未知

A prospective, nonrandomized, noninterventional study to compare Nexfin CO-trek cardiac output with thermodilution cardiac output

Edwards Lifesciences LLC0 个研究点目标入组 55 人开始时间: 2015年9月10日最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
55

研究概览

简要总结

2018 results in https://pubmed.ncbi.nlm.nih.gov/29239149/ (added 12/05/2021)

研究设计

研究类型
Observational

入排标准

性别
All

入选标准

  • 1. Subjects must be at least 18 years of age
  • 2. Subjects must give signed written informed consent
  • 3. Subjects' height and weight must be accurately obtained prior to study start

排除标准

  • 1. Aortic or tricuspid 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
  • 8. Patients being treated with an intra-aortic balloon pump
  • 9. Patient is currently participating in an investigational drug or another device study that clinically interferes with the study endpoints

研究者

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