[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100565122":3},{"organization":4,"armGroups":7,"interventions":7,"overallOfficials":7,"centralContacts":8,"locations":14,"responsibleParty":32,"collaborators":34,"id":45,"slug":7,"hasResults":46,"nctId":47,"briefTitle":48,"officialTitle":48,"acronym":7,"eligibilityCriteria":49,"healthyVolunteers":46,"sex":50,"minAge":51,"maxAge":7,"enrollmentInfo":52,"targetDuration":7,"studyType":55,"phases":7,"briefSummary":56,"conditions":57,"keywords":7,"overallStatus":17,"whyStopped":7,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":69},{"fullName":5,"class":6},"Medtronic - MITG","INDUSTRY",null,[9],{"name":10,"role":11,"phone":12,"phoneExt":7,"email":13},"Elise Huisman","CONTACT","+1 236-308-4876","elise.huisman@medtronic.com",[15],{"facility":16,"status":17,"city":18,"state":19,"zip":20,"country":21,"cosmosGeoPoint":22,"geoPoint":27,"contacts":28},"Saint Pauls Hospital","RECRUITING","Vancouver","British Columbia","V6Z 1Y6","Canada",{"type":23,"coordinates":24},"Point",[25,26],-123.11934,49.24966,{"lat":26,"lon":25},[29],{"name":30,"role":11,"phone":7,"phoneExt":7,"email":31},"Ronald Ree, MD","rree@providencehealth.bc.ca",{"type":33,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR",[35,38,40,42],{"name":36,"class":37},"Excelar","UNKNOWN",{"name":39,"class":6},"Cloud DX Inc.",{"name":41,"class":37},"Bridge Health Solutions",{"name":43,"class":44},"Providence Healthcare","OTHER","100565122",false,"NCT06638073","Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Continuous Vitals Monitoring - Department of Anesthesia at PHC","Inclusion Criteria:\n\n* 19 years or older\n* Patients that have undergone a non-cardiac surgery at SPH requiring an inpatient hospital stay\n* Peri-op patients who are in the Surgical High Acuity Unit (SHAU) and those followed by Anesthesia Perioperative Outreach team on the ward\n* Living within British Columbia, Canada and in an area that is covered by Bell cellular network\n\nExclusion Criteria:\n\n* Patient refusal\n* Lack of capacity to consent to the study (including having received sedative or general anesthetic within the past 24 hours)\n* Unable to use (or does not have a caregiver who can help put on) study monitoring device at home\n* Unable to complete (or does not have a caregiver who can help complete) study questionnaires by electronic (mobile, tablet, or computer), paper, nor phone\n* No access to cell phone nor landline at home to receive follow-ups\n* Preoperatively known to be discharged to a nursing home or rehabilitation facility\n* Known allergic reactions to any part material of study devices","ALL","19 Years",{"count":53,"type":54},50,"ESTIMATED","OBSERVATIONAL","To confirm feasibility and accessibility of the CCPC Platform (Oxymotion, Bridge Health Solutions medication adherence software, CloudDX home kit) in two different environments - in hospital and at-home, in patients undergoing non-cardiac surgery.",[58,59],"Surgical Procedure, Unspecified","Intensive Care Units (ICUs)","2026-03-10",{"date":62,"type":63},"2026-03-12","ACTUAL",{"date":65,"type":63},"2025-03-13",{"date":67,"type":54},"2026-06-20",{"name":5,"class":6},1]