ECMO ABI Detection With Hyperfine
Key facts
- Where
- Kansas City, United StatesSee the site
Where in United States
- Children's MercyKansas City, United StatesTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Children's Mercy Hospital Kansas City
- Trial code
- NCT06469801
- Record updated
- 24 September 2026
- Original description
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.Read full original descriptionShow less
Low-Field Bedside MRI for Detection of Acute Brain Injury in Pediatric Extracorporeal Membrane Oxygenation
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.
Inclusion: 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: 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; Pregnancy; Any patient who has a contraindication to having an MRI.