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Clinical Trial Summary

The study primarily aims to collect standard of care clinical data in a wide spectrum of simple to complex mitral valve regurgitation (MVR) cases to validate a post-processing stand-alone software prototype (QFlow), developed by Philips Research Paris (Medisys). Investigator does not intervene in the care of the patient, but simply collects standard of care images and measurements that are needed for the validation of the investigational software.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03286088
Study type Interventional
Source Philips Electronics Nederland B.V. acting through Philips CTO organization
Contact
Status Completed
Phase N/A
Start date August 22, 2017
Completion date December 31, 2019