Daily ECMO check: could a simple protocol save lives and money?
NCT ID NCT05486559
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a daily, step-by-step assessment could help doctors safely remove patients from a life-support machine called ECMO sooner. 225 adults on ECMO were randomly assigned to either the daily protocol or usual care. The goal was to see if the protocol shortened the time on ECMO without increasing risks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- daily assessment protocol for readiness to stop ECMO
- What this could lead to
- If successful, this protocol could help doctors safely remove patients from ECMO sooner, reducing complications and hospital costs.
- What could go wrong
- This is a completed trial, but the approach may not work for all patients or hospitals. The study is relatively small (225 people) and focused on one type of ECMO.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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225 people
The number who actually took part.
- Started
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Sep 2022
- Finished
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May 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient receiving VV-ECMO * Patient is located in a participating unit of an adult hospital Exclusion Criteria: * Patient is pregnant * Patient is a prisoner * Patient is \< 18 years old * Participant is receiving ECMO as bridge to transplant * Participant is receiving a hybrid configuration that includes an arterial cannula * Patient has received VV-ECMO for \> 48 hours
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Baylor University Medical Center
Dallas, Texas, 75246, United States
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Hennepin County Medical Center
Minneapolis, Minnesota, 55415, United States
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Stanford University
Stanford, California, 94305, United States
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Texas Tech University Health Sciences Center of El Paso
El Paso, Texas, 79905, United States
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Toronto General Hospital
Toronto, Ontario, M5G 2C4, Canada
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UC San Diego Health
San Diego, California, 92037, United States
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University of Utah Health
Salt Lake City, Utah, 84112, United States
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Vanderbilt University Medical Center
Nashville, Tennessee, 37232, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Blood test may forecast life-threatening clots or bleeds on ECMO
- Portable MRI could spot brain injury in children on life support
- ECMO Patients' hidden infection risk under the microscope
- ECMO breakthrough? major trial aims to cut deadly complications
- New study aims to uncover why ECMO patients bleed
- ECMO blood thinner showdown: which drug wins?