[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100548651":3},{"organization":4,"armGroups":7,"interventions":7,"overallOfficials":7,"centralContacts":8,"locations":14,"responsibleParty":41,"collaborators":45,"id":48,"slug":7,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":55,"sex":56,"minAge":57,"maxAge":7,"enrollmentInfo":58,"targetDuration":7,"studyType":61,"phases":7,"briefSummary":62,"conditions":63,"keywords":7,"overallStatus":28,"whyStopped":7,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":74},{"fullName":5,"class":6},"Brigham and Women's Hospital","OTHER",null,[9],{"name":10,"role":11,"phone":12,"phoneExt":7,"email":13},"Samuel B Snider, MD","CONTACT","857-307-2391","ssnider@bwh.harvard.edu",[15,27],{"facility":5,"status":16,"city":17,"state":18,"zip":19,"country":20,"cosmosGeoPoint":21,"geoPoint":26,"contacts":7},"ACTIVE_NOT_RECRUITING","Boston","Massachusetts","02115","United States",{"type":22,"coordinates":23},"Point",[24,25],-71.05977,42.35843,{"lat":25,"lon":24},{"facility":5,"status":28,"city":29,"state":18,"zip":30,"country":20,"cosmosGeoPoint":31,"geoPoint":35,"contacts":36},"RECRUITING","Brookline","02114",{"type":22,"coordinates":32},[33,34],-71.12116,42.33176,{"lat":34,"lon":33},[37],{"name":38,"role":11,"phone":39,"phoneExt":7,"email":40},"Sam Snider","9196142137","ssnider@partners.org",{"type":42,"investigatorFullName":43,"investigatorTitle":44,"investigatorAffiliation":5,"oldNameTitle":7,"oldOrganization":7},"PRINCIPAL_INVESTIGATOR","Samuel Snider, MD","Principal Investigator, Assistant Professor of Neurology at Brigham and Women's Hospital",[46],{"name":47,"class":6},"American Heart Association","100548651",false,"NCT06423768","fMRI in CardiaC arrEst With Uncertain Prognosis","The fMRI in CardiaC arrEst With Uncertain Prognosis (FACE-UP) Study","FACE-UP","Inclusion Criteria:\n\n* survive of an in or out of hospital cardiac arrest\n\nExclusion Criteria:\n\n* Drug overdose\n* Opinion of medical team patient unlikely to survive more than 24 hours (severe concurrent medical illness, dilated and unreactive pupils, etc..)\n* Following verbal commands (MD or RN note) once TTM is complete and normothermia is achieved (Day 2 or 3; Day of admission is Hospital Day 0). If no TTM is administered, this can be assessed on Hospital Day 2.\n* Following verbal commands (study team assessment) at time of MRI\n* Family planning to WLST at time of enrollment\n* Non English speaker (okay if English not primary language, as long as they can understand it)\n* Permanent Contraindication to MRI (some kind of implanted metal)\n* Pregnant",true,"ALL","18 Years",{"count":59,"type":60},50,"ESTIMATED","OBSERVATIONAL","The goal of this observational study is to determine whether specific advanced MRI measures are associated with functional outcomes in patients who are comatose after cardiac arrest. The main question\\[s\\] it aims to answer are:\n\nAim 1: Determine if stimulus-based functional MRI (fMRI)-measured activations are independently associated with favorable neurological outcomes after cardiac arrest\n\nAim 2: Determine if resting state functional MRI (rs-fMRI)-measured functional network connectivity is independently associated with favorable neurological outcomes after cardiac arrest.\n\nAim 3: Determine if diffusion tensor imaging (DTI)-measured white matter integrity is associated with favorable neurological outcomes after cardiac arrest.\n\nParticipants will undergo advanced MRI sequences at time of clinical MRI, and will be followed for 6 months post-arrest.",[64],"Cardiac Arrest","2026-06-18",{"date":67,"type":68},"2026-06-22","ACTUAL",{"date":70,"type":68},"2024-05-16",{"date":72,"type":60},"2027-12-01",{"name":5,"class":6},2]