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Therapy and Outcome of Prolonged Veno-venous ECMO Therapy of Critically Ill ARDS Patients.

G

Goethe University

Status

Completed

Conditions

Extracorporeal Membrane Oxygenation Complication
Outcome, Fatal

Treatments

Other: Outcome

Study type

Observational

Funder types

Other

Identifiers

NCT05338593
prolonged VV-ECMO

Details and patient eligibility

About

In the context of the coronavirus (COVID-19) pandemic, healthcare systems worldwide faced an unprecedented shortage of severe ARDS. Critically affected patients were treated with veno-venous extracorporeal membrane oxygenation (VV-ECMO) for complete respiratory failure early in the pandemic. Due to a shortage of resources in the sense of terminal equipment and adequately trained personnel with appropriate expertise in many countries and regions, a strict selection of suitable patients was made. Repeatedly, it was observed that patients under VV-ECMO also needed several weeks to recover sufficiently to generate device sufficient gas exchange. Due to the scarcity of VV-ECMO resources outside of the pandemic, the question arose whether a prolonged therapy still holds a sufficient prospect of success and what the course of treatment of such patients would be like.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

veno-venous extracorporeal membrane oxygenation

Exclusion criteria

veno-arterial extracorporeal membrane oxygenation

Trial design

100 participants in 1 patient group

prolonged veno-venous extracorporeal membrane oxygenation
Description:
Critically affected patients treated with veno-venous extracorporeal membrane oxygenation (VV-ECMO). Based on severe acute respiratory distress syndrome (ARDS) and prolonged therapy for more than 2 weeks.
Treatment:
Other: Outcome

Trial contacts and locations

1

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Central trial contact

Armin N Flinspach, MD.; Elisabeth H Adam, MD.

Data sourced from clinicaltrials.gov

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