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Perioperative Smartwatch Monitoring to Predict Complications — PreSmart  

Post-Op Complication Clinical Trial

Official title:
Perioperative Smartwatch Monitoring as a Tool to Predict Post-operative Complications in Patients Undergoing Major Abdominal Surgery. A Single Center Prospective Observational Study.

Clinical Trial Summary

This is a prospective, single-center, observational study designed to to quantify complications following major visceral surgery major visceral surgery (such as pancreatic resection or colorectal colorectal surgery), and to identify digital biomarkers (collected pre, and post-operatively by a connected watch) enabling early early identification of patients with post-operative complications. Patients will be invited to wear a watch during the perioperative period, and will receive questionnaires about their their health status.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06156033
Study type Observational
Source Centre Hospitalier Universitaire Vaudois
Contact Benoit Henry
Phone 0798828587
Email benoit.henry@chuv.ch
Status Not yet recruiting
Phase
Start date January 1, 2024
Completion date August 2024
View Details
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