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Clinical Trial Summary

A prospective, multicenter, uncontrolled study to evaluate the safety and efficacy of the Cardiapex percutaneous trans-apical access and closure system. The Cardiapex device intended for percutaneous access and closure of the left ventricular apex in conjunction with transapical Transcatheter Aortic Valve Implantation (TAVI).


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label


Related Conditions & MeSH terms

  • Transapical Transcatheter Aortic Valve Implantation

NCT number NCT01722591
Study type Interventional
Source Cardiapex Ltd.
Contact
Status Terminated
Phase N/A
Start date January 2013