[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100528074":3},{"organization":4,"armGroups":7,"interventions":7,"overallOfficials":8,"centralContacts":12,"locations":22,"responsibleParty":47,"collaborators":7,"id":50,"slug":7,"hasResults":51,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":51,"sex":57,"minAge":58,"maxAge":7,"enrollmentInfo":59,"targetDuration":7,"studyType":62,"phases":7,"briefSummary":63,"conditions":64,"keywords":7,"overallStatus":66,"whyStopped":7,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":76},{"fullName":5,"class":6},"Centre Hospitalier Universitaire Vaudois","OTHER",null,[9],{"name":10,"affiliation":5,"role":11},"Patrick Schoettker, Prof","STUDY_DIRECTOR",[13,18],{"name":14,"role":15,"phone":16,"phoneExt":7,"email":17},"Bastien Morleo","CONTACT","+41 79 556 59 93","bastien.morleo@chuv.ch",{"name":19,"role":15,"phone":20,"phoneExt":7,"email":21},"Magnus Olofsson","+41 79 556 38 09","magnus.olofsson@chuv.ch",[23],{"facility":24,"status":7,"city":25,"state":26,"zip":27,"country":28,"cosmosGeoPoint":29,"geoPoint":34,"contacts":35},"CHUV","Lausanne","Canton of Vaud","1011","Switzerland",{"type":30,"coordinates":31},"Point",[32,33],6.63282,46.516,{"lat":33,"lon":32},[36,40,43,44],{"name":37,"role":15,"phone":38,"phoneExt":7,"email":39},"Henry Benoit","+41798828587","benoit.henry@chuv.ch",{"name":41,"role":42,"phone":7,"phoneExt":7,"email":7},"Magnus Olofsson, MD","SUB_INVESTIGATOR",{"name":37,"role":42,"phone":7,"phoneExt":7,"email":7},{"name":45,"role":46,"phone":7,"phoneExt":7,"email":7},"Schoettker Patrick, PD-MD","PRINCIPAL_INVESTIGATOR",{"type":46,"investigatorFullName":48,"investigatorTitle":49,"investigatorAffiliation":5,"oldNameTitle":7,"oldOrganization":7},"Patrick Schoettker","Prof. and Head of department (anesthesiology)","100528074",false,"NCT06156033","Perioperative Smart Device Monitoring to Predict Complications","Perioperative Smart Device Monitoring as a Tool to Predict Post-operative Complications in Patients Undergoing Non Cardiac Intermediate and High-risk Surgery. A Single-center Prospective Observational Study","PreSmart","Patients will be recruited prospectively for a total of 50 patients.\n\nInclusion criteria are :\n\n* Patients scheduled for elective non cardiac intermediate or high-risk surgery under general anesthesia\n* 18 years of age or older\n* Capacity to understand french language\n\nExclusion criteria will be :\n\n\\- Patient refusal and\u002For inability to understand and sign informed consent","ALL","18 Years",{"count":60,"type":61},50,"ESTIMATED","OBSERVATIONAL","This is a prospective, single-center, observational study designed to to quantify complications following non cardiac intermediate and high-risk surgery, and to identify digital biomarkers (collected pre, and post-operatively by a connected device) enabling early early identification of patients with post-operative complications. Patients will be invited to wear a smartdevice during the perioperative period, and will receive questionnaires about their their health status.",[65],"Post-Op Complication","NOT_YET_RECRUITING","2026-03-24",{"date":69,"type":70},"2026-03-27","ACTUAL",{"date":72,"type":61},"2026-04-01",{"date":74,"type":61},"2027-03",{"name":5,"class":6},1]