[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100583932":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":19,"centralContacts":23,"locations":10,"responsibleParty":31,"collaborators":10,"id":33,"slug":34,"hasResults":35,"nctId":36,"briefTitle":37,"officialTitle":37,"acronym":10,"eligibilityCriteria":38,"healthyVolunteers":35,"sex":39,"minAge":40,"maxAge":10,"enrollmentInfo":41,"targetDuration":10,"studyType":44,"phases":10,"briefSummary":45,"conditions":46,"keywords":48,"overallStatus":55,"whyStopped":10,"lastUpdateSubmitDate":56,"lastUpdatePostDateStruct":57,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":10},{"fullName":5,"class":6},"University Health Network, Toronto","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Cardiac surgery patients",null,"Adult patients undergoing cardiac surgery on cardiopulmonary bypass at Toronto General Hospital",[13],"Other: No intervention (observational study)",[15],{"type":6,"name":16,"description":17,"armGroupLabels":18,"otherNames":10},"No intervention (observational study)","This is an observational study. No intervention.",[9],[20],{"name":21,"affiliation":5,"role":22},"Keyvan Karkouti","PRINCIPAL_INVESTIGATOR",[24,29],{"name":21,"role":25,"phone":26,"phoneExt":27,"email":28},"CONTACT","416-340-4800","8597","keyvan.karkouti@uhn.ca",{"name":30,"role":25,"phone":10,"phoneExt":10,"email":10},"Deep Grewal",{"type":32,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100583932","relationship-of-point-of-care-coagulation-assays-with-clinical-outcomes-in-cardiac-surgery-a-retrospective-cohort-study-100583932",false,"NCT06882759","Relationship of Point-of-care Coagulation Assays with Clinical Outcomes in Cardiac Surgery: a Retrospective Cohort Study","Inclusion Criteria:\n\n* Adult patients ≥ 18 years old\n* Underwent a cardiac surgical procedure with cardiopulmonary bypass\n\nExclusion Criteria:\n\n\\- Did not undergo viscoelastic testing during surgery","ALL","18 Years",{"count":42,"type":43},15000,"ESTIMATED","OBSERVATIONAL","The goal of this observational study is to determine the relationship of ROTEM point-of-care coagulation assay parameters with excessive bleeding and clinical outcomes in patients undergoing cardiac surgery at Toronto General Hospital. The main questions it aims to answer are: i) How well does viscoelastic testing (VET) predict the clinical outcome of excessive bleeding in cardiac surgery? ii) Which VET parameters have the greatest accuracy for identification of patients who will have excessive bleeding? iii) 3) What is the prognostic value of abnormal VET parameters with other clinical outcomes after cardiac surgery?",[47],"Cardiac Surgery Requiring Cardiopulmonary Bypass",[49,50,51,52,53,54],"cardiac surgery","viscoelastic testing","point-of-care","ROTEM","cardiopulmonary bypass","bleeding","NOT_YET_RECRUITING","2025-03-14",{"date":58,"type":59},"2025-03-19","ACTUAL",{"date":61,"type":43},"2025-03-15",{"date":63,"type":43},"2026-03-15",{"name":5,"class":6}]