Portable brain scans could speed up ER diagnoses
NCT ID NCT06930534
First seen Jun 25, 2026 · Last updated Sep 03, 2026 · Updated 3 times
Summary
This study tested whether a portable MRI scanner can start scans faster than a conventional MRI in emergency patients. 100 adults in the ER who needed a brain MRI were randomly assigned to get a portable scan plus standard care, or standard care alone. Researchers measured the time from when the MRI was ordered to when the scan actually began.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Swoop Plus Mk2.0 portable brain MRI scanner
- What this could lead to
- If portable MRI is faster, it could help emergency departments diagnose brain conditions more quickly, potentially speeding up treatment.
- What could go wrong
- This is a small, completed study focused on scan timing, not on patient outcomes. Portable MRI may not detect all findings as well as conventional 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
-
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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100 people
The number who actually took part.
- Started
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Apr 2025
- 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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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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Male or female ≥ 18 years of age at presentation to Yale New Haven Hospital Adult ED * Order to receive conventional brain MRI imaging originating in the YNHH Adult ED Exclusion Criteria: * Lack of assent from treating physician for inclusion in this protocol. * Contraindications to 1.5T MRI evaluation, including: 1. Cardiac Pacemaker or defibrillator 2. Aneurysm clip 3. Implants or devices attached to the body in the chest or above, such as: 1. Nerve stimulator 2. Deep brain stimulator 3. Programmable shunt 4. Stent 5. Pain pump 6. Artificial extremity 4. Implants in the ears (hearing aid or cochlear implant 5. Any shrapnel, pellets, bullets, metallic fragments, or other metallic foreign body above the chest 6. Metallic joints, rods, screws, or other orthopedic implants in or above the chest 7. Braces, dentures, removable teeth, or dental expanders that cannot be removed. 8. Body piercings in or above the chest that cannot be removed. 9. MRI-incompatible Tracheostomy tube or Swan Ganz catheter in place 10. Status Epilepticus or anyone previously seizing deemed by the physician not to be suitable for pMRI
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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
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Yale New Haven Health Emergency Department
New Haven, Connecticut, 06520, United States
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