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 sites120 target enrollmentTBD

Conditionsspecifieke aandoeningen zijn niet van belang voor het onderzoek daar het onderzoek in een cardiologische omgeving uitgevoerd zal worden, zullen meeste proefpersonen cardiologische aandoeningen hebben N.A.

Overview

Phase: N/A
Intervention: Not specified
Conditions: specifieke aandoeningen zijn niet van belang voor het onderzoek
Sponsor: Edwards Lifesciences LLC
Enrollment: 120
Status: Completed
Last Updated: 2 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

No summary available.

Registry

who.int

Start Date

TBD

End Date

TBD

Last Updated

2 years ago

Study Type

Interventional

Investigators

Sponsor

Edwards Lifesciences LLC

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

•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.

Outcomes

Primary Outcomes

Not specified

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