ECMO ABI Detection With Hyperfine

Recruiting now · Not applicable

Conditions studied: Acute Brain Injury, Extracorporeal Membrane Oxygenation Complication, Hypoxia-Ischemia, Brain, Stroke, Acute

In brief

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.

Key facts

Study ID

NCT06469801

Run by

Children's Mercy Hospital Kansas City

People needed

30

Starts

2024-07-23

Expected to finish

2027-12-01

Last updated by the study team

2026-07-01

Who can join

Age: any, up to 17. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

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
• Passive implants are considered MRI-conditional

Where it is running

• Children's Mercy — Kansas City, Missouri, United States (enrolling)

Full record on ClinicalTrials.gov

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