Trials / Completed
CompletedNCT01777815
Safety and Performance Study of the NeoChord Device
Safety and Performance Study of the NeoChord Suturing Device in Subjects With Degenerative Mitral Valve Disease; Diagnosed With Severe Mitral Regurgitation
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 30 (actual)
- Sponsor
- NeoChord · Industry
- Sex
- All
- Age
- 18 Years – 79 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | NeoChord DS1000 Artificial Chordae Delivery System |
Timeline
- Start date
- 2009-10-01
- Primary completion
- 2012-10-01
- Completion
- 2014-08-01
- First posted
- 2013-01-29
- Last updated
- 2014-09-25
Locations
8 sites across 4 countries: Denmark, Germany, Italy, Lithuania
Source: ClinicalTrials.gov record NCT01777815. Inclusion in this directory is not an endorsement.