Bicentric Study on the Use of ECMO-VV or VA for Severe ARDS Associated With Covid-19 (ECMO-SL-CoV-2)

University Hospital, Strasbourg, France

Status: Completed

Conditions: Covid-19

Study type: Observational

Funder types: Other

Identifiers

NCT04446286

7904

Details and patient eligibility

About

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

Enrollment: 50 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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