Condition: Aortic Stenosis · Coronary Artery Disease · TAVI · Sponsor: University of Zurich
The primary objective of this study is to compare, in patients with severe aortic stenosis and concomitant coronary artery disease accepted for transcatheter aortic valve implantation (TAVI) and percutaneous coronary intervention (PCI) by the multidisciplinary Heart Team, the safety and efficacy of angiography-guided complete revascularization performed after (within 1-45 days) with angiography-guided complete revascularization performed before (within 1-45 days) TAVI using the Edwards SAPIEN Transcatheter Heart Valve®.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| Klinikum Klagenfurt am Wörthersee | Klagenfurt, Austria | — |
| University Hospital Dijon | Dijon, France | — |
| The Clinique de l'Infirmerie Protestante | Lyon, France | — |
| Cardiology Department, CHU Timone Marseille | Marseille, France | — |
| Arnault Tzanck Institute Saint Laurent du Var | Nice, France | — |
| Toulouse University Hospital | Toulouse, France | — |
| Zentralklinik Bad Berka | Bad Berka, Germany | — |
| Heart and Vascular Centre Bad Bevensen | Bad Bevensen, Germany | — |
| Universitäts-Herzzentrum Freiburg Bad Krozingen, Freiburg & Bad Krozingen | Bad Krozingen, Germany | — |
| Campus Kerckhoff of the Justus Liebig University Giessen | Bad Nauheim, Germany | — |
| Cardiovascular Center Bad Neustadt/Saale | Bad Neustadt an der Saale, Germany | — |
| Schüchtermann-Clinic Bad Rothenfelde | Bad Rothenfelde, Germany | — |
+ 36 more locations — full list on the registry record.
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