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ECMO Braile Biomédica® in COVID-19 Patients (ECMO_COVID)

B

Braile Biomedica

Status

Enrolling

Conditions

COVID-19

Treatments

Device: Patients underwent cardiorespiratory support

Study type

Observational

Funder types

Industry

Identifiers

NCT06086405
ECMO COVID

Details and patient eligibility

About

Retrospective data collection to evaluate the gas transfer capacity of the Braile Biomédica® OxyPrime® ECMO BRCoating® Membrane Oxygenator in COVID-19 patients during the pandemic.

Full description

Multicenter, retrospective, non-comparative, non-randomized study to assess the clinical performance of the OxyPrime® ECMO BRCoating® Membrane Oxygenator in adult patients with COVID-19

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients ≥ 18 years old, with a previous diagnosis of COVID-19, who were placed on ECMO using the Oxyprime® ECMO Braile Biomédica® Membrane Oxygenator, from March 2020 to July 2022, following the Instructions for Use (IFU) of the products.

Exclusion criteria

  • Patients without a diagnosis of COVID-19

Trial contacts and locations

1

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Central trial contact

Glacia G Basso; Priscila C Joao

Data sourced from clinicaltrials.gov

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