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Clinical Trial Summary

The study will evaluate all female patients with severe aortic stenosis undergoing transcatheter valve implantation with commercially available valves and delivery systems.


Clinical Trial Description

WINTAVI is an international, multi-centre, prospective, observational registry. The purpose of this study is to collect 'real-world' data regarding the clinical utility of all commercially available Transcatheter Aortic Valve Implantation (TAVI) devices for percutaneous aortic valve implantation in female patients with severe Aortic Stenosis (AS) requiring treatment. Data collected in this study will provide additional information on the understanding of the safety and device performance in a 'real-world' setting and how to best treat patients with severe AS. This will include Quality of Life questionnaires (KCCQ). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01819181
Study type Observational [Patient Registry]
Source Icahn School of Medicine at Mount Sinai
Contact
Status Completed
Phase
Start date March 2013
Completion date April 26, 2018

See also
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