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Place of ECMO in the Management of Severe Refractory ARDS Associated With Covid-19

STUDY ECMO-COVID-19 : Place of ECMO in the Management of Severe Refractory ARDS Associated With Covid-19

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04343404
Acronym
ECMO-COVID-19
Enrollment
100
Registered
2020-04-13
Start date
2020-04-01
Completion date
2020-04-15
Last updated
2020-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Respiratory Distress Syndrome

Keywords

Respiratory Distress Syndrome, ARDS, SARS-COV-2, Extracorporeal membrane oxygenation, ECMO, Veno-venous ECMO

Brief summary

Describe COVID-19 patients who are receiving ECMO-VV respiratory replacement and what happens to them.

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

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 during hospitalisation; * Patient agreeing to participate in the study

Exclusion criteria

* Sujet under guardianship or trusteeship * Sujet under safeguard of justice

Design outcomes

Primary

MeasureTime frame
Retrospective description of COVID-19 patients receiving respiratory ECMO-VV supplementation and what happens to themFiles analysed retrospectily from March 1st, 2020 to April 15, 2020 will be examined

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026