[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100551968":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":7,"centralContacts":12,"locations":22,"responsibleParty":41,"collaborators":7,"id":43,"slug":7,"hasResults":44,"nctId":45,"briefTitle":46,"officialTitle":46,"acronym":47,"eligibilityCriteria":48,"healthyVolunteers":44,"sex":49,"minAge":50,"maxAge":7,"enrollmentInfo":51,"targetDuration":7,"studyType":54,"phases":7,"briefSummary":55,"conditions":56,"keywords":59,"overallStatus":24,"whyStopped":7,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":72},{"fullName":5,"class":6},"Centre Hospitalier Sud Francilien","OTHER",null,[9],{"type":6,"name":10,"description":11,"armGroupLabels":7,"otherNames":7},"Ventilator associated event","Measure of incidence of Ventilator associated event",[13,18],{"name":14,"role":15,"phone":16,"phoneExt":7,"email":17},"Fabrice COOK, MD","CONTACT","01 61 69 52 28","fabrice.cook@chsf.fr",{"name":19,"role":15,"phone":20,"phoneExt":7,"email":21},"Caroline TOURTE","01 61 69 31 50","caroline.tourte@chsf.fr",[23],{"facility":5,"status":24,"city":25,"state":7,"zip":26,"country":27,"countryCode":28,"cosmosGeoPoint":29,"geoPoint":34,"contacts":35},"RECRUITING","Corbeil-Essonnes","91106","France","FR",{"type":30,"coordinates":31},"Point",[32,33],2.48757,48.60603,{"lat":33,"lon":32},[36,38],{"name":19,"role":15,"phone":37,"phoneExt":7,"email":21},"0161693730",{"name":39,"role":40,"phone":7,"phoneExt":7,"email":7},"Fabrice COOK","PRINCIPAL_INVESTIGATOR",{"type":42,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100551968",false,"NCT06466980","Study of Ventilator Associated Event During Intensive Care After Resuscitated Cardiac Arrest.","VAE-ACR","Inclusion Criteria:\n\n* Adult male or female\n* Non-pregnant female\n* Successfully resuscitated from cardiac arrest during primary care\n* Invasive mechanical ventilation initiated during resuscitation and continued for at least 4 days\n* No decision to limit life-sustaining therapies within 24 hours following admission to intensive care\n* No requirement of arteriovenous circulatory support during intensive care management\n\nExclusion Criteria\n\n\\- patients who opposed to the use of their data","ALL","18 Years",{"count":52,"type":53},150,"ESTIMATED","OBSERVATIONAL","The aim is to describe the incidence, characteristics, risk factors and outcome of complications acquired under mechanical ventilation (called ventilator-associated events) according to the new CDC criteria, in a population of patients admitted in intensive care unit after cardiac arrest.",[57,58],"Cardiac Arrest With Successful Resuscitation","Mechanical Ventilation",[10,60,61,62],"cardiac arrest","ventilator-acquired pneumonia","ventilator associated pneumonia","2025-03-12",{"date":65,"type":66},"2025-03-14","ACTUAL",{"date":68,"type":66},"2024-06-27",{"date":70,"type":53},"2025-12-31",{"name":5,"class":6},1]