Breethe Abiomed Recovery RegisTry (BART)
NCT05473130 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 48
Last updated 2024-09-04
Summary
The BART Registry intended to utilize observational data of the Abiomed Breethe OXY-1 System™ in real-world settings to drive best practice usage patterns, serve as a tool to measure and improve the quality of patient care and as a resource to inform us on the design of future studies.
Conditions
- Cardiopulmonary Bypass
- ARDS
- Heart Failure
Interventions
- DEVICE
-
Breethe Oxy-1 System
To pump, oxygenate, and remove carbon dioxide from blood during cardiopulmonary bypass with Breethe Oxy-1 System
Sponsors & Collaborators
-
Abiomed Inc.
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-03-31
- Primary Completion
- 2024-04-02
- Completion
- 2024-04-02
- FDA Device
- Yes
Countries
- United States
Study Locations
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