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Clinical Trial Summary

Study is aimed to demonstrate that the self-expandable Allegra TAVI system provides lower mean gradient assessed by TTE compared to balloon-expandable valve systems in a female patient population with symptomatic severe aortic stenosis


Clinical Trial Description

Study is aimed to demonstrate that the self-expandable Allegra transcatheter aortic valve implantation (TAVI) system provides lower mean gradient assessed by Transthoracic Echo (TTE) at 30 days post procedure, compared to balloon-expandable valve systems in a female patient population with symptomatic severe aortic stenosis. Patients in both arm will receive anticoagulants according to routine practice of the hospital. Patients will be followed-up until 1 year after the procedure. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05989074
Study type Interventional
Source Ceric Sàrl
Contact Nozomi Watanabe
Phone +33 (0)6 61 38 94 80
Email nwatanabe@cerc-europe.org
Status Not yet recruiting
Phase N/A
Start date February 1, 2024
Completion date August 31, 2025