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

Launched by UNIVERSITY HOSPITAL TUEBINGEN · Dec 19, 2019

Trial Information

Current as of July 25, 2025

Recruiting

Keywords

Acute Respiratory Distress Syndrome Extracorporal Membrane Oxygenation Outcome Ventilation Therapy Qol

ClinConnect Summary

The Early Versus Late Initiation of ECMO (ELIEO-Trial) is a research study designed to find out whether starting a treatment called Extracorporeal Membrane Oxygenation (ECMO) right away or waiting until conservative treatments fail is better for patients with Acute Respiratory Distress Syndrome (ARDS). ARDS is a serious lung condition that makes it hard to breathe. In this trial, patients who develop ARDS will be assigned to either receive ECMO immediately upon entering the intensive care unit or to receive standard treatments first, with the option of starting ECMO later if needed. The goal is to see which approach helps patients recover better.

To be eligible for this trial, participants must be adults aged 18 and older who have been diagnosed with ARDS within the past 7 days and are enrolled within 96 hours of their symptoms beginning. They should also be willing to receive full intensive care support. If someone participates, they can expect to be monitored closely until they leave the hospital. It’s important to note that this trial is not yet recruiting participants, so it’s still in the planning stages.

Gender

ALL

Eligibility criteria

  • 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

About University Hospital Tuebingen

University Hospital Tübingen is a leading academic medical institution in Germany, renowned for its commitment to advancing healthcare through innovative research and clinical excellence. As a prominent sponsor of clinical trials, the hospital leverages its multidisciplinary expertise and cutting-edge facilities to develop new therapeutic strategies and improve patient outcomes. With a strong focus on translational medicine, University Hospital Tübingen collaborates with various stakeholders, including pharmaceutical companies and research organizations, to facilitate the efficient and ethical conduct of trials across a wide range of medical disciplines. Their dedication to patient-centered research and rigorous scientific standards positions them at the forefront of medical advancements.

Locations

Tübingen, , Germany

Patients applied

0 patients applied

Trial Officials

Peter Rosenberger, Prof.

Principal Investigator

University Hospital Tübingen

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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