Baby-Sized MRI machine could spot brain injuries in kids on ECMO without moving them
NCT ID NCT06074406
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a portable, low-field MRI machine could safely scan the brains of children (ages 0-17) who are on ECMO, a type of life support. The goal was to see if the bedside scan was feasible and safe, not to treat or cure any condition. Twenty children participated, and researchers measured things like side effects, scan time, and staff needed.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Hyperfine portable low-field MRI device
- What this could lead to
- If successful, this could make it easier and safer to scan the brains of critically ill children on ECMO without moving them to a traditional MRI machine.
- What could go wrong
- This is a very small, early feasibility study with only 20 participants. It does not test whether the scans improve outcomes, and the image quality may be lower than standard MRI.
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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20 people
The number who actually took part.
- Started
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Aug 2023
- Finished
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Dec 2025
- 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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Up to 17 years
- 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 * Subjects admitted to the Pediatric Intensive Care Unit, Cardiac Intensive Care Unit, or the Neonatal Intensive Care Unit at Children's Mercy Kansas City * Ages 0-17 years * Undergoing venovenous or venoarterial ECMO Exclusion Criteria * Pregnancy * Active implants such as: * Pacemaker * Implanted defibrillator * Implanted insulin pump * Deep brain stimulator * Vagus nerve stimulator * Cochlear implant * Programmable shunt * MRI incompatible surgical hardware (e.g., staples, screws, etc.) * Metal-containing tattoos or permanent make-up on head or neck * Suspected metal in eye, e.g., * Former or current welders, metal workers, or individuals with a metal injury * Metal shrapnel * Passive implants are considered MRI conditional
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Children's Mercy Kansas City
Kansas City, Missouri, 64108, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Blood test may forecast life-threatening clots or bleeds on ECMO
- Common ICU procedure may briefly raise brain pressure — study investigates the risk