Other Clinical Trial - Assessment of St Jude Medical Portico Re-sheathable

Updated 06/21/2024

Status Withdrawn

Clinical Trial Summary

The purpose of this study is to assess the safety and performance of the 23mm Portico Transcatheter Heart Valve and the TAVI Transapical Delivery System in subjects with severe symptomatic aortic stenosis

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Aortic Valve Stenosis
Constriction, Pathologic
Severe Symptomatic Aortic Stenosis

Clinical Trial Details

NCT number	NCT01742598
Study type	Interventional
Source	Abbott Medical Devices
Contact
Status	Withdrawn
Phase	N/A
Start date	December 2015
Completion date	November 2020

See also
	Status	Clinical Trial	Phase
	Not yet recruiting	`NCT02210351` - Evaluation of Association Between Apical Dysfunction and Trans Apical Access for TAVR, in Patients With Severe Aortic Stenosis, Undergoing Trans Apical Trans Catheter Aortic Valve Replacement (TAP-TAVR).	N/A
	Completed	`NCT02956915` - Evaluation of Length of Stay After TF-TAVI
	Recruiting	`NCT05326126` - Microvascular Function in Patients Undergoing Transcatheter Aortic Valve Implant (TAVI) for Severe Symptomatic Aortic Stenosis: Association With Myocardial Fibrosis	N/A
	Completed	`NCT04663334` - Change in Coronary Microcirculation and FFR After TAVI in Patients With Cardiovascular Comorbidities
	Withdrawn	`NCT01927601` - Assessment of Neurologic Injury Subsequent to Transcatheter Aortic Valve Replacement: A Feasibility Study	N/A
	Completed	`NCT01787084` - Alternative Access Approaches for Transcatheter Aortic Valve Replace (TAVR) in Inoperable Patients With Aortic Stenosis	N/A