Assessing Brain Injury Using Portable Magnetic Resonance Imaging (MRI)
Completed
Conditions studied: Extracorporeal Membrane Oxygenation Complication, Acute Brain Injury
In brief
This study aims to assess the feasibility of assessing acute brain injury using a portable low field MRI in patients on ECMO.
Key facts
- Study ID
- NCT05469139
- Run by
- Johns Hopkins University
- People needed
- 50
- Starts
- 2021-12-10
- Expected to finish
- 2024-03-11
- Last updated by the study team
- 2024-03-13
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults age 18 and over
- Patient supported with extracorporeal membrane oxygenation support (ECMO)
- Legally authorized representative has provided written informed consent
You may not qualify if…
- Patient has a contraindication for MRI such as:
- Implants such as pacemaker, defibrillator, implanted insulin pump, deep brain stimulator, vagus nerve stimulator, cochlear implant, or programmable shunt
- MRI incompatible surgical hardware such as staples, screws. ferromagnetic implants such as aneurysm clips, surgical clips, prostheses, cochlear implant
- artificial hearts or heart valves with steel parts
- metal fragments
- shrapnel
- tattoos near the eye
- permanent make-up
- steel implants
- or other irremovable ferromagnetic objects
- Patient weight is over 440 lbs (or 200kg)
- Patient has Intra Aortic Balloon Pump (IABP), Implanted Ventricular Assist Device (VAD), or Percutaneous Ventricular Assist Device
- Patient is pregnant
Where it is running
- Johns Hopkins Hospital — Baltimore, Maryland, United States
- University of Texas Health Science Center — Houston, Texas, United States
Full record on ClinicalTrials.gov
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