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Clinical Trial Summary

Non-significant risk device study to conduct evaluation of the performance of new device for monitoring of cardiac function (based on previous iterations 510(k) 173156)


Clinical Trial Description

This validation study will help to establish feasibility of using the CPS monitor to screen patients for ejection fraction (EF), CO, PASP and wedge pressure compared to a standard echocardiogram. No clinical decisions will be made as a result of the CPS device EF value and this measurement will be taken for comparison purposes only. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05104307
Study type Observational
Source University of Pittsburgh
Contact
Status Completed
Phase
Start date November 9, 2021
Completion date January 2, 2024

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