Early Feasibility Study of the Edwards APTURE Transcatheter Shunt System
Sponsor: Edwards Lifesciences • ClinicalTrials.gov ID: NCT07858799
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The objectives of this early feasibility study are to: evaluate initial clinical safety, device functionality, and effectiveness of the APTURE system for treatment of symptomatic HFrEF patients with elevated LAP, provide guidance for future clinical study and system designs utilizing the APTURE system.
Interventions
-
Edwards APTURE transcatheter shunt system
(Device)
Transcatheter treatment of symptomatic heart failure patients with elevated left atrial pressure (LAP).
Eligibility criteria
Conditions
Locations
- Herzzentrum Universitätsklinikum Köln — Cologne, Germany, Germany
- Herzzentrum Dresden GmbH Universitätsklinik für Innere Medizin und Kardiologie — Dresden, Germany, Germany
- Johannes Gutenberg Universitaet Mainz — Mainz, Germany, Germany
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Learn MoreOfficial Source
Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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