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RECRUITING
NCT04782232
Registry to Assess the Safety and Feasibility of the Subpulmonary Support with the Novel Venous Cannula in Patients with Failing/Absence of the Right Heart
Sponsor: Berlin Heart GmbH
View on ClinicalTrials.gov
Summary
The purpose of the study is to monitor the clinical safety and performance of the EXCOR Venous Cannula in context of an EXCOR VAD therapy to ensure continued acceptability of identified risks, to enable detecting emerging risks and to assess clinical improvement on both short- and long-term.
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
20
Start Date
2021-06-01
Completion Date
2027-09
Last Updated
2025-02-17
Healthy Volunteers
No
Conditions
Interventions
OTHER
No intervention
No intervention due to observational design
Locations (1)
LMU Klinikum
Munich, Germany