[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"infection-without-sepsis\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:infection-without-sepsis":41},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":12,"acronym":13,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":21,"conditions":22,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100616051",false,"NCT07300579","Vascular Events in Noncardiac Surgery Patients Cohort Evaluation Study 2","VISION-2","Inclusion Criteria:\n\n1. age ≥65 years;\n2. underwent non-cardiac surgery with general, neuraxial, local, or regional anesthesia; and\n3. expected length of hospital stay of 3 or more days\n\nExclusion Criteria:\n\n1. hearing aid(s) or cochlear implant(s) in left ear;\n2. pacemaker\u002Fimplantable cardioverter-defibrillator (ICD);\n3. externally programmable cerebrospinal fluid shunt;\n4. deep brain stimulator;\n5. intolerance\u002Fallergy to adhesive;\n6. history of dementia, or;\n7. previous enrollment in the VISION-2 Study","ALL","65 Years",{"count":18,"type":19},20000,"ESTIMATED","OBSERVATIONAL","VISION-2 is an international, multi-site, prospective observational cohort study of 20,000 patients undergoing noncardiac surgery. Continuous biometric data will be blindly collected for the first 30 postoperative days, in hospital and at home, using Vitaliti™. Following study enrollment and baseline data collection, follow up visits will occur in-hospital, at 30-days, and 1-year post-operatively.\n\nVISION-2 has 3 primary objectives, among participants who underwent noncardiac surgery, the investigators will: 1) determine the pattern and frequency of physiological precursors (i.e., biophysical signals) to MINS, BIMS, sepsis, and infection without sepsis; 2) build prediction models from these biophysical signals and their extracted features through supervised machine learning, for the prediction and early detection of those complications; and 3) build a biobank for evaluation of novel biomarkers.",[23,24,25,26,27],"Myocardial Injury After Noncardiac Surgery (MINS)","Bleeding Independently Associated With Mortality After Noncardiac Surgery (BIMS)","Sepsis","Infection Without Sepsis","Post-operative Complications","NOT_YET_RECRUITING","2026-04-09",{"date":31,"type":32},"2026-04-14","ACTUAL",{"date":34,"type":19},"2026-06",{"date":36,"type":19},"2032-06",{"name":38,"class":39},"Hamilton Health Sciences Corporation","OTHER",3,""]