Portable MRI to detect brain injury after cardiac arrest
Official title: Prospective Identification of Hypoxic Ischemic Brain Injury Using Portable Magnetic Resonance Imaging
Run by Yale University · NCT07197918 · Data updated 2026-11-12
This will test whether a bedside portable MRI can detect hypoxic-ischemic brain injury in adults who are unresponsive after resuscitation from cardiac arrest.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Yale University Academic / other |
| Locations | 1 site (New Haven, Connecticut) |
| Status | Recruiting |
| Started | December 2, 2025 |
| Main results expected | April 2027 |
| Study ends | April 2027 |
| Registry record updated | January 27, 2026 |
| Trial ID | NCT07197918 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults (≥18) who remain unresponsive after in- or out-of-hospital cardiac arrest, are receiving temperature control, and for whom conventional MRI is clinically indicated.
✕Probably not a fit
Patients with standard MRI contraindications, inability to tolerate 30 minutes supine, clear diffuse severe injury on early CT, or who are already awake are unlikely to benefit from this imaging-focused study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study compares low-field portable MRI performed at the bedside with conventional high-field MRI to measure the severity of hypoxic-ischemic brain injury after cardiac arrest. Investigators will obtain early portable MRI scans within 6 and 24 hours after return of spontaneous circulation and perform serial imaging over subsequent days to track injury evolution. The study measures inter-rater agreement between readers and the specificity and positive predictive value of early diffusion-weighted imaging lesions versus conventional MRI and clinical outcomes. Enrollment is at a single center and focuses on adults receiving temperature control who are unresponsive after cardiac arrest.
Why it matters
Potential benefit: If successful, portable MRI could enable safer bedside brain imaging at hospitals without high-field scanners, reduce risky transports, and help identify patients most likely to benefit from therapies or clinical trials.
How similar studies have gone: Early feasibility studies of low-field portable MRI in critical care settings have shown promise for bedside imaging, but this approach has not been widely validated specifically for predicting hypoxic-ischemic brain injury after cardiac arrest.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Unresponsive immediately after ROSC from IHCA or OHCA * Age ≥ 18 years of age * Conventional MRI is clinically indicated * Treatment with temperature control Exclusion Criteria: * MRI contraindication according to the American Heart Association guidelines * Inability to tolerate supine positioning for 30 minutes * Diffuse loss of grey-white differentiation and sulcal effacement on head computed tomography within 6 hours of ROSC
Where it's running
-
Yale New Haven Hospital
New Haven, Connecticut, United States Recruiting
Study contacts
- Principal investigator: Rachel Beekman, MD — Yale University
- Study coordinator: Rachel Beekman, MD
- Email: rachel.beekman@yale.edu
- Phone: 516-965-4251
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.