Perioperative Smart Device Monitoring to Predict Complications
ConditionPost-Op Complication
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Hospitalier Universitaire Vaudois
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.
Patients scheduled for elective non cardiac intermediate or high-risk surgery under general anesthesia
18 years of age or older
Capacity to understand french language
None