Cardiovascular Disease Clinical Trial
Official title:
A Clinical Study of the CardiAQ™ Transcatheter Mitral Valve Implantation (TMVI) System (Transapical Delivery System)
NCT number | NCT02478008 |
Other study ID # | CIP-3102-01 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | June 17, 2015 |
Last updated | September 9, 2015 |
Start date | June 2015 |
The purpose of the study is to evaluate the initial short and long-term safety and
performance of the CardiAQ™ Transcatheter Mitral Valve Implantation System using the
Transapical Delivery System.
The study will enroll patients with moderate to severe mitral valve regurgitation who are
considered high or extreme risk for mortality and morbidity from conventional open heart
surgery.
Status | Recruiting |
Enrollment | 60 |
Est. completion date | |
Est. primary completion date | December 2016 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 65 Years and older |
Eligibility |
Key Inclusion Criteria: - NYHA Classification = III - Left Ventricular Ejection Fraction = 30% - Mitral regurgitation = Grade 3+ - Subject meets anatomical eligibility criteria for the investigational device |
Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Denmark | Rigshospitalet University Hospital | Copenhagen | |
France | Centre hospitalier régional universitaire de Lille | Lille | |
France | Hôpital Européen Georges-Pompidou | Paris | |
France | Centre Hospitalier Universiatier de Toulouse | Toulouse | |
Netherlands | Medisch Centrum Leeuwarden | Leeuwarden | |
Netherlands | St. Antonius Ziekenhuis | Nieuwegein | |
Netherlands | Erasmus University Medical Center | Rotterdam | |
United Kingdom | Leeds General Infirmary | Leeds | |
United Kingdom | New Cross Hospital Heart Center | Wolverhampton |
Lead Sponsor | Collaborator |
---|---|
CardiAQ Valve Technologies, Inc. |
Denmark, France, Netherlands, United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Composite Major Adverse Event Rate | 30-Day | Yes | |
Primary | Composite Major Adverse Event Rate | 12-Month | Yes |
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