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Breethe Abiomed Recovery RegisTry (BART)

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Abiomed

Status

Completed

Conditions

Cardiopulmonary Bypass
Heart Failure
ARDS

Treatments

Device: Breethe Oxy-1 System

Study type

Observational

Funder types

Industry

Identifiers

NCT05473130
11202020

Details and patient eligibility

About

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.

Enrollment

48 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • all adult subjects supported with Breethe Oxy-1 System

Exclusion criteria

  • subjects under 18 years of age

Trial contacts and locations

6

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Data sourced from clinicaltrials.gov

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