[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100608158":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":24,"locations":33,"responsibleParty":48,"collaborators":50,"id":54,"slug":55,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":10,"eligibilityCriteria":60,"healthyVolunteers":56,"sex":61,"minAge":62,"maxAge":10,"enrollmentInfo":63,"targetDuration":10,"studyType":66,"phases":10,"briefSummary":67,"conditions":68,"keywords":10,"overallStatus":36,"whyStopped":10,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":80},{"fullName":5,"class":6},"Yale University","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Cardiac arrest with Return of Spontaneous Circulation (ROSC)",null,"All enrolled patients will have two to three portable MRIs ( \\\u003C6 hours, 6-24 hours and one within 12 (+\u002F- 12) hours of conventional MRI) and one conventional MRI. Standard of care will occur per the clinical team and this study will not interfere with standard of care.",[13],"Device: portable MRI scanner",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":10},"DEVICE","portable MRI scanner","Participants will receive 2-3 portable MRI scans: \\\u003C6 hours, 6-24 hours, and within 12 (+\u002F- 12) hours of conventional MRI",[9],[21],{"name":22,"affiliation":5,"role":23},"Rachel Beekman, MD","PRINCIPAL_INVESTIGATOR",[25,29],{"name":22,"role":26,"phone":27,"phoneExt":10,"email":28},"CONTACT","516-965-4251","rachel.beekman@yale.edu",{"name":30,"role":26,"phone":31,"phoneExt":10,"email":32},"Emily Gilmore, MD, MS","203-314-0555","emily.gilmore@yale.edu",[34],{"facility":35,"status":36,"city":37,"state":38,"zip":39,"country":40,"countryCode":41,"cosmosGeoPoint":42,"geoPoint":47,"contacts":10},"Yale New Haven Hospital","RECRUITING","New Haven","Connecticut","05620","United States","US",{"type":43,"coordinates":44},"Point",[45,46],-72.92816,41.30815,{"lat":46,"lon":45},{"type":49,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR",[51],{"name":52,"class":53},"National Institute of Neurological Disorders and Stroke (NINDS)","NIH","100608158","identification-of-brain-injury-using-portable-mri-100608158",false,"NCT07197918","Identification of Brain Injury Using Portable MRI","Prospective Identification of Hypoxic Ischemic Brain Injury Using Portable Magnetic Resonance Imaging","Inclusion Criteria:\n\n* Unresponsive immediately after ROSC from IHCA or OHCA\n* Age ≥ 18 years of age\n* Conventional MRI is clinically indicated\n* Treatment with temperature control\n\nExclusion Criteria:\n\n* MRI contraindication according to the American Heart Association guidelines\n* Inability to tolerate supine positioning for 30 minutes\n* Diffuse loss of grey-white differentiation and sulcal effacement on head computed tomography within 6 hours of ROSC","ALL","18 Years",{"count":64,"type":65},60,"ESTIMATED","OBSERVATIONAL","The goal of this study is to look for brain injury in patients who had a cardiac arrest, using portable brain imaging. The portable nature of this test will also allow for serial imaging so the investigators can understand how brain injury changes over days. The results of this study may allow for bedside imaging to be available at centers without specialized imaging centers and may identify markers of brain injury that help to select the patients most likely to benefit for clinical trials.",[69,70],"Cardiac Arrest (CA)","Hypoxic-Ischemic Brain Injury","2026-01-26",{"date":73,"type":74},"2026-01-27","ACTUAL",{"date":76,"type":74},"2025-12-02",{"date":78,"type":65},"2027-04",{"name":5,"class":6},1]