No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
Up to 17
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
200 (estimated)
Sponsor
Children's Mercy Hospital Kansas City · Other
Who this trial is looking for
This trial is looking for children aged 0-17 who might have brain injuries due to lack of oxygen. Participants will receive a portable MRI to help doctors understand their condition better.
Are You a Good Fit for This Trial?
You may be able to join if
I am hospitalized in a Pediatric Intensive Care Unit or similar unit.
I am between 0 and 17 years old.
I have an acute neurologic issue suspected to be due to brain injury or am at high risk for it.
You may not be able to join if
I am pregnant.
I cannot have an MRI for medical reasons.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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 …
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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 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 fo…
Inclusion Criteria:
* 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
Exclusion Criteria:
* Pregnancy
* Any patient who has a contraindication to having an MRI
Patients with a passive or active implant will:
* First be reviewed on MRISafety.com to determine MR conditionality
* If the device is listed as Conditional or Unsafe for a 1.5T or a 3T, the device will then be reviewed by the MRI Safety Officer or MRI Physician Section chief to determine true conditionality for the portable MRI
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