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Bicentric Study on the Use of ECMO-VV or VA for Severe ARDS Associated With Covid-19

Bicentric Study on the Use of ECMO-VV or VA for Severe ARDS Associated With Covid-19

Recruiting
18 years and older
All
Phase N/A

Overview

Describes the cohort of patients receiving ECMO-VV or ECMO-VA in the management of severe ARDS refractory to SARS-CoV-2 in the Strasbourg and Louvain centres

Eligibility

Inclusion Criteria:

  • Patient over the age of 18;
  • Diagnostic COVID-19 by RT-PCR;
  • Hospitalisation in resuscitation for the management of complications related to COVID-19
  • Implanted ECMO-VV or VA during hospitalisation;
  • Patient agreeing to participate in the study

Exclusion Criteria:

  • Sujet who has expressed opposition to participating in the study.
  • Sujet under guardianship or trusteeship
  • Sujet under safeguard of justice

Study details
    Covid 19

NCT04446286

University Hospital, Strasbourg, France

5 August 2020

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