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

  • STATUS
    Recruiting
  • participants needed
    50
  • sponsor
    University Hospital, Strasbourg, France
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Updated on 5 August 2020
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resuscitation
respiratory distress
covid-19
SARS
acute respiratory distress
acute respiratory syndrome (sars)

Summary

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

Details
Condition Covid 19
Age 18years - 100years
Clinical Study IdentifierNCT04446286
SponsorUniversity Hospital, Strasbourg, France
Last Modified on5 August 2020

Eligibility

 Yes No Not Sure

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
Clear my responses
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