Clinical Trials Directory

Trials / Unknown

UnknownNCT00677638

Transapical Implantation of Ventor Embracer™ Valve in Patients With Severe Aortic Valve Disease

Catheter-Based Transapical Implantation of the Ventor Embracer™ Heart Valve Prosthesis in Patients With Severe Aortic Valve Disease

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Ventor Technologies · Industry
Sex
All
Age
75 Years
Healthy volunteers
Not accepted

Summary

A prospective single arm study evaluating feasibility and safety of a catheter-based transapical implantation of the Ventor Embracer™ aortic valve bioprosthesis in patients with severe aortic valve disease, specifically aortic stenosis, who are at elevated risk for standard surgical valve replacement.

Conditions

Interventions

TypeNameDescription
DEVICEVentor EmbracerImplantation of Ventor Embracer

Timeline

Start date
2008-06-01
Primary completion
2010-01-01
Completion
2014-12-01
First posted
2008-05-14
Last updated
2009-12-03

Locations

3 sites across 1 country: Germany

Source: ClinicalTrials.gov record NCT00677638. Inclusion in this directory is not an endorsement.