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ECMO ABI Detection With Hyperfine

RecruitingNAAges 0 Days - 17 YearsAllChildren's Mercy Hospital Kansas City
NCT06469801 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The primary objective is to characterize the prevalence and type of ABI following cannulation for pediatric patients who require ECMO support. The secondary objective is to describe the time course and rates of ABI using ultralow-field bedside MRI relative to both duration of ECMO support and clinical imaging obtained in routine care of pediatric ECMO patients.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Participants that will be or are admitted to the Pediatric Intensive Care Unit, Cardiac Intensive Care Unit, or the Neonatal Intensive Care Unit * Ages 0-17 years * Participants that are at high risk for undergoing ECMO or are currently undergoing venovenous or venoarterial ECMO • High risk participants include, but are not limited to: * Undergoing cardiac surgery * Congenital heart disease * Congenital diaphragmatic hernia * Refractory hypoxemic and/or hypercarbic respiratory failure * Vasoactive-refractory shock 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 device is listed as Conditional or Unsafe for a 1.5T or a 3T, device will then be reviewed by MRI Safety Officer or MRI Physician Section chief to determine true conditionality for the portable MRI
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What it tests

  • Hyperfine
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Where

1 site
Children's Mercy
Kansas City, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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