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Safety and Performance Study of the NeoChord Device — TACT  

Mitral Valve Regurgitation Clinical Trial

Official title:
Safety and Performance Study of the NeoChord Suturing Device in Subjects With Degenerative Mitral Valve Disease; Diagnosed With Severe Mitral Regurgitation

Clinical Trial Summary

The purpose of this study is to demonstrate the safety and performance of the NeoChord DS1000 Artificial Chordae Delivery System in implanting ePTFE sutures(s) as artificial neochordae in patients with mitral regurgitation.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01777815
Study type Interventional
Source NeoChord
Contact
Status Completed
Phase N/A
Start date October 2009
Completion date August 2014
View Details
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