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NCT04343404 Clinical Trial

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

Respiratory Distress Syndrome Clinical Trial

— ECMO-COVID-19  

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04343404
Other study ID # 7772
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 1, 2020
Est. completion date April 15, 2020

Study information
Verified date April 2020
Source University Hospital, Strasbourg, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date April 15, 2020
Est. primary completion date April 15, 2020
Accepts healthy volunteers
Gender All
Age group 18 Years and older
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 during hospitalisation;

- Patient agreeing to participate in the study

Exclusion Criteria:

- Sujet under guardianship or trusteeship

- Sujet under safeguard of justice

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Service de Chirurgie Thoracique Nouvel Hôpital Civil Hôpitaux Universitaires de Strasbourg Strasbourg

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Retrospective description of COVID-19 patients receiving respiratory ECMO-VV supplementation and what happens to them Files analysed retrospectily from March 1st, 2020 to April 15, 2020 will be examined
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