Portico TAVI Implant With Transfemoral Delivery System

Status Completed

Clinical Trial Summary

The purpose of this study is to assess the safety and effectiveness of the SJM Portico Transcatheter Heart Valve and the SJM TAVI Transfemoral Transcatheter delivery system in subjects with severe symptomatic aortic stenosis (AS).

Clinical Trial Description

Data will be collected at baseline, procedure, discharge, 30 days post implant, 3 months post implant, 6 months post implant, and 12 months post implant. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01493284
Study type	Interventional
Source	Abbott Medical Devices
Contact
Status	Completed
Phase	N/A
Start date	December 2011
Completion date	September 2016

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See also
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