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Clinical Trial Summary

The study purpose is to evaluate the safety and feasibility of the CORolla™ TAA in two treatment groups, "CORolla™ Stand-alone group" and " AVR & CORolla™ Add on group".


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Safety Study, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01956526
Study type Interventional
Source CorAssist Cadiovascular Ltd.
Contact Lea Lak, M.D.
Phone +972 9 9554500
Email lea@corassist.com
Status Recruiting
Phase N/A
Start date August 2013
Completion date September 2017