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CompletedNCT04446286ECMO-SL-CoV-2Updated Oct 8, 2021

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

An observational study in Covid-19, sponsored by University Hospital, Strasbourg, France. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2021-10-08.

Sponsored by University Hospital, Strasbourg, France · Observational

Study type
Observational
Model
Case-only
Time perspective
Other
Enrollment
50
Ages
18 Years and older
Sex
All
01

Study 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

02

Conditions studied

  • Covid-19

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Keywords

  • Respiratory Distress Syndrome
  • SARS-CoV-2
  • Extracorporeal membrane oxygenation
  • ECMO-VV
  • ECMO-VA
  • Veno-venous ECMO
03

In context

COVID-19

7,640 studies on the registry are indexed under COVID-19; 488 are open to participants now.

This study's enrollment of 50 is below the median of 261 across 3,136 observational studies indexed under COVID-19.

Browse COVID-19 studies →

Lead sponsor

University Hospital, Strasbourg, France is the lead sponsor of 966 studies on the registry; 342 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Adult patients with a COVID-19 diagnosis by RT-PCR

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

Exclusion Criteria:

  • Sujet who has expressed opposition to participating in the study.
  • Sujet under guardianship or trusteeship
  • Sujet under safeguard of justice
05

Study design

Observational model
Case-only
Time perspective
Other
Enrollment
50 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Retrospective description of effect of the ECMO-VV or ECMO-VA in the management of severe ARDS refractory in patients of the Strasbourg and Louvain centres with covid-19

    Time frame: files analysed retrospectily from March 1st, 2020 to August 1st, 2020 will be examined

07

Study locations

1 site
  • Service de Chirurgie Thoracique Nouvel Hôpital Civil Hôpitaux Universitaires de Strasbourg
    Strasbourg, 67091, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 8, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04446286
Lead sponsor
University Hospital, Strasbourg, France
Responsible party
Sponsor
First posted
Jun 24, 2020
Start date
Jun 18, 2020
Primary completion
Aug 18, 2020
Completion
Aug 18, 2020
Last update
Oct 8, 2021

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2020. You cannot join it, but the record below documents what was studied.

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