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Clinical Trials in Germany / NCT04208126
Recruiting Not applicable

Early Versus Late Initiation of ECMO (Extracorporal Membrane Oxygenation) Trial (ELIEO-Trial)

NCT04208126 · tracked via the Priya Life Science Germany tracker
Phase
Not applicable
Started
2025-03-01
Last updated
2025-05-23

Condition(s) studied

Acute Respiratory Distress Syndrome

Investigational drug(s) / intervention(s)

ECMO

ECMO: ECMO implantation immediately after ICU admission

Study summary

This trial is a prospective randomized multicenter trial that assigns patients to either a treatment for Acute Respiratory Distress Syndrome (ARDS) with an Extracorporal Membrane Oxygenation (ECMO) immediately after admission to the intensive care unit or conservative treatment. The later can undergo ECMO following failure of conservative therapy as a rescue therapy. Patients will be included within 24 hours of the onset of symptoms of ARDS and will be randomized according to standard procedure. Follow-up will be performed until day 90 after study inclusion.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * ARDS as defined according to the Berlin Definition1 * The term "acute onset" is defined as follow: the duration of the hypoxemia criterion and the chest radiograph criterion must be ≤ 7 days at the time of randomization. * Patients must be enrolled within 96 hours of onset of ARDS and no later than 7 days from the initiation of mechanical ventilation. Exclusion Criteria: * Age less than 18 years * More than 7 days since initiation of mechanical ventilation * more than 96 hours since meeting inclusion criteria * patient, surrogate or physician not committed to full intensive care support * pregnancy

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University hospital Tübingen Tübingen Germany Recruiting

More University Hospital Tuebingen trials in Germany

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04208126 on ClinicalTrials.gov ↗ ← All trials in Germany