Low-Field Bedside Brain Magnetic Resonance Imaging in Pediatric Extracorporeal Membrane Oxygenation

Not Applicable

Active, not recruiting

• Conditions: Feasibility and Safety of a Low-field MRI; Acute Brain Injury; Extracorporeal Membrane Oxygenation Complication

• Registration Number: NCT06074406
• Lead Sponsor: Children's Mercy Hospital Kansas City

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-9-4
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Active, not recruiting
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

Inclusion Criteria<br><br> - Subjects admitted to the Pediatric Intensive Care Unit, Cardiac Intensive Care Unit,<br> or the Neonatal Intensive Care Unit at Children's Mercy Kansas City<br><br> - Ages 0-17 years<br><br> - Undergoing venovenous or venoarterial ECMO<br><br>Exclusion Criteria<br><br> - Pregnancy<br><br> - Active implants such as:<br><br> - Pacemaker<br><br> - Implanted defibrillator<br><br> - Implanted insulin pump<br><br> - Deep brain stimulator<br><br> - Vagus nerve stimulator<br><br> - Cochlear implant<br><br> - Programmable shunt<br><br> - MRI incompatible surgical hardware (e.g., staples, screws, etc.)<br><br> - Metal-containing tattoos or permanent make-up on head or neck<br><br> - Suspected metal in eye, e.g.,<br><br> - Former or current welders, metal workers, or individuals with a metal injury<br><br> - Metal shrapnel<br><br> - Passive implants are considered MRI conditional

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Examining the occurrence of adverse events and serious adverse events with portable MRI use in ECMO patients;Assessing the time needed to conduct a portable MRI with ECMO patients.;Analyzing the number of staff required to conduct a Portable MRI with an ECMO patient.;Determine the number of critical care therapies conducted during imaging studies.