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POLESTAR Trial - An International Multi-center Early Discharge TAVI Program — POLESTAR  

Aortic Valve Stenosis Clinical Trial

Official title:
Project to Look for Early Discharge in Patients Undergoing TAVI With ACURATE - An International Multi-center Early Discharge TAVI Program

Clinical Trial Summary

An international multi-center prospective observational study to address safety and feasibility of an early discharge protocol in patients with symptomatic severe aortic stenosis who are eligible for transfemoral TAVI with the Boston Scientific ACURATE Neo Aortic Bioprosthesis transcatheter heart valve.

Clinical Trial Description

In this International multi-center prospective observational study, 250 patients with severe symptomatic aortic stenosis (AS) and eligibility for transfemoral TAVI with ACURATE Neo Bioprosthesis, will be pre-procedurally selected for participation in an early discharge protocol in which patients are discharged within 48 hours after uncomplicated TAVI. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03910751
Study type Observational [Patient Registry]
Source Erasmus Medical Center
Contact
Status Active, not recruiting
Phase
Start date April 1, 2019
Completion date February 1, 2024
View Details
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