[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100556027":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":26,"locations":34,"responsibleParty":113,"collaborators":10,"id":115,"slug":116,"hasResults":117,"nctId":118,"briefTitle":119,"officialTitle":120,"acronym":121,"eligibilityCriteria":122,"healthyVolunteers":117,"sex":123,"minAge":124,"maxAge":125,"enrollmentInfo":126,"targetDuration":10,"studyType":129,"phases":10,"briefSummary":130,"conditions":131,"keywords":134,"overallStatus":37,"whyStopped":10,"lastUpdateSubmitDate":136,"lastUpdatePostDateStruct":137,"startDateStruct":140,"completionDateStruct":142,"leadSponsor":144,"locationsCount":145},{"fullName":5,"class":6},"Population Health Research Institute","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Study Cohort",null,"Participants will receive up to 14 days of continuous cardiac monitoring",[13],"Device: Cardiac monitoring device",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":10},"DEVICE","Cardiac monitoring device","Portable, up to 14 days of monitoring",[9],[21,24],{"name":22,"affiliation":5,"role":23},"David Conen, MD, MPH","PRINCIPAL_INVESTIGATOR",{"name":25,"affiliation":5,"role":23},"Michael K Wang, MD",[27,32],{"name":28,"role":29,"phone":30,"phoneExt":10,"email":31},"Vitheya Thanabalan","CONTACT","+1 905-296-2710","detectpoaf@phri.ca",{"name":33,"role":29,"phone":10,"phoneExt":10,"email":31},"Kate Brady",[35,57,67,76,88,100],{"facility":36,"status":37,"city":38,"state":39,"zip":40,"country":41,"countryCode":42,"cosmosGeoPoint":43,"geoPoint":48,"contacts":49},"Hamilton General Hospital","RECRUITING","Hamilton","Ontario","L8L 2X2","Canada","CA",{"type":44,"coordinates":45},"Point",[46,47],-79.84963,43.25011,{"lat":47,"lon":46},[50,55],{"name":51,"role":29,"phone":52,"phoneExt":53,"email":54},"Research Coordinator","905-521-2100","44156","gregus@hhsc.ca",{"name":56,"role":29,"phone":10,"phoneExt":10,"email":10},"Mohamed Panju, MD",{"facility":58,"status":59,"city":38,"state":39,"zip":60,"country":41,"countryCode":42,"cosmosGeoPoint":61,"geoPoint":63,"contacts":64},"St. Joseph's Healthcare Hamilton","NOT_YET_RECRUITING","L8N 4A6",{"type":44,"coordinates":62},[46,47],{"lat":47,"lon":46},[65],{"name":66,"role":29,"phone":10,"phoneExt":10,"email":10},"Vikas Tandon, MD",{"facility":68,"status":37,"city":38,"state":39,"zip":69,"country":41,"countryCode":42,"cosmosGeoPoint":70,"geoPoint":72,"contacts":73},"Juravinski Hospital","L8V 1C3",{"type":44,"coordinates":71},[46,47],{"lat":47,"lon":46},[74],{"name":75,"role":29,"phone":10,"phoneExt":10,"email":10},"Ameen Patel, MD",{"facility":77,"status":59,"city":78,"state":39,"zip":79,"country":41,"countryCode":42,"cosmosGeoPoint":80,"geoPoint":84,"contacts":85},"London Health Sciences Centre - University Hospital","London","N6A 5A5",{"type":44,"coordinates":81},[82,83],-81.23304,42.98339,{"lat":83,"lon":82},[86],{"name":87,"role":29,"phone":10,"phoneExt":10,"email":10},"Marko Mrkobrada, MD",{"facility":89,"status":59,"city":90,"state":39,"zip":91,"country":41,"countryCode":42,"cosmosGeoPoint":92,"geoPoint":96,"contacts":97},"Niagara Health System - St. Catharine's Site","St. Catharines","L2S 0A9",{"type":44,"coordinates":93},[94,95],-79.24267,43.17126,{"lat":95,"lon":94},[98],{"name":99,"role":29,"phone":10,"phoneExt":10,"email":10},"Leonard Blair, MD",{"facility":101,"status":59,"city":102,"state":103,"zip":104,"country":41,"countryCode":42,"cosmosGeoPoint":105,"geoPoint":109,"contacts":110},"Hôpital Fleurimont du Centre hospitalier universitaire de Sherbrooke","Sherbrooke","Quebec","J1H 5H3",{"type":44,"coordinates":106},[107,108],-71.89908,45.40008,{"lat":108,"lon":107},[111],{"name":112,"role":29,"phone":10,"phoneExt":10,"email":10},"Félix Ayala-Paredes, MD",{"type":114,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100556027","detection-of-perioperative-atrial-fibrillation-after-noncardiac-surgery-100556027",false,"NCT06519747","DETECTion of PeriOperative Atrial Fibrillation After Noncardiac Surgery","Enhanced DETECTion of PeriOperative Atrial Fibrillation After Noncardiac Surgery with Continuous Electrocardiographic Monitoring","DETECT-POAF","Inclusion Criteria:\n\n1. Had undergone noncardiac surgery within the past 72 hours and requiring, or expected to require, at least one of the following:\n\n   * an overnight hospital admission after surgery\n   * day surgery that would result in a large enough physiological insult to be able to cause POAF. Procedures excluded include those that are conducted using local anesthesia alone, are less than 30 minutes in duration, and\u002For are judged to be of low physiologic insult by the local investigator.\n2. Have one of the following high-risk criteria;\n\n   * age 55-64 years, and having either established cardiovascular disease, recent major vascular surgery, a CHA2DS2-VASc score ≥3, or an elevated postoperative troponin level;\n   * age 65-74 years, and having either established cardiovascular disease, recent major vascular surgery, a CHA2DS2-VASc score ≥2, or an elevated postoperative troponin level; or\n   * age ≥75 years;\n3. Provide written informed consent to participate.\n\nExclusion Criteria:\n\n1. History of documented chronic (i.e., non-transient) AF before noncardiac surgery;\n2. Need for long-term systemic anticoagulation;\n3. Ongoing need for long-term dual antiplatelet treatment;\n4. Contraindication to oral anticoagulation;\n5. Severe renal insufficiency;\n6. Severe liver cirrhosis;\n7. Acute stroke in the past 14 days;\n8. Underwent cardiac surgery in the past 35 days;\n9. History of nontraumatic intracranial, intraocular, or spinal bleeding;\n10. Hemorrhagic disorder or bleeding diathesis;\n11. Known life expectancy \\\u003C1 year due to concomitant disease;\n12. Women who are pregnant, breastfeeding, or of childbearing potential not taking effective contraception;\n13. Expected to be non-compliant with follow-up and\u002For device use;\n14. Known contact allergy to monitoring device and\u002For its peripheral components;\n15. Previously enrolled in DETECT-POAF.","ALL","18 Years","120 Years",{"count":127,"type":128},750,"ESTIMATED","OBSERVATIONAL","This is a multicentre prospective cohort study where patients will receive up to 14 days of continuous ECG monitoring by wearing a portable monitoring device, starting within 72 hours after noncardiac surgery.",[132,133],"Atrial Fibrillation","Atrial Flutter",[135],"Cardiac monitoring","2024-11-05",{"date":138,"type":139},"2024-11-07","ACTUAL",{"date":141,"type":139},"2024-10-15",{"date":143,"type":128},"2026-12-31",{"name":5,"class":6},6]