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Clinical Trial Summary

Prospective, observational, multi-center trial in which patients with mitral regurgitation sufficient to merit mitral valve repair will receive a surgical transvalvular, intra-annular Mitral Bridgeâ„¢ to reduce or eliminate mitral regurgitation.


Clinical Trial Description

The primary objective of this study is to evaluate the safety and performance of the Mitral Bridge device in the correction of mitral valve regurgitation in patients who qualify for mitral valve repair as defined by the American Society of Echocardiography (ASE). The device is a single use, mitral valve implant designed to reduce mitral regurgitation by reducing the septo-lateral mitral annular diameter, promoting early coaptation of the valve leaflets and restraining the leaflets below the intra-annular plane.

The protocol was designed as a First In Man (FIM) with a 6-month follow up but was amended to follow the enrolled patients for a total of 5 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03511716
Study type Observational
Source Heart Repair Technologies, Inc.
Contact
Status Terminated
Phase
Start date February 6, 2014
Completion date August 31, 2019

See also
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