Portable MRI for Pediatric Hypoxic Ischemic Brain Injury
Recruiting now · Not applicable
Conditions studied: Acute Brain Injury, Hypoxia, Brain, Ischemia, Brain, Brain Injuries, Trauma, Brain, Stroke
In brief
This study will evaluate the sensitivity and specificity of low field portable MRI (pMRI) for detection of hypoxic ischemic brain injuries in pediatric patients compared to clinically obtained neuroimaging to define pediatric diagnostic limitations and to determine the diagnostic capabilities of this neuroimaging modality following optimization of image acquisition. The results of this study will help determine optimal clinical implementation opportunities in pediatric patients.
Key facts
- Study ID
- NCT07577336
- Run by
- Children's Mercy Hospital Kansas City
- People needed
- 200
- Starts
- 2026-07-06
- Expected to finish
- 2027-12-01
- Last updated by the study team
- 2026-07-08
Who can join
Age: any, up to 17. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients hospitalized in the Pediatric Intensive Care Unit, Cardiac Intensive Care Unit, or the Neonatal Intensive Care Unit
- Ages 0-17 years at study enrollment
- Acute neurologic deficit suspected secondary to Hypoxic Ischemic Brain Injury (HIBI) or patients at high risk for HIBI
You may not qualify if…
- 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
Where it is running
- Children's Mercy Hospital and Clinics — Kansas City, Missouri, United States (enrolling)
Full record on ClinicalTrials.gov
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