Enhanced Vitals Monitoring After Major Surgery Trial

NANot yet recruitingINTERVENTIONAL
Enrollment

110

Participants

Timeline

Start Date

September 3, 2024

Primary Completion Date

February 28, 2025

Study Completion Date

March 31, 2025

Conditions
SurgeryPost Operative ComplicationsQuality of RecoveryGeneral SurgeryVascular SurgeryUrologyGynecology
Interventions
DEVICE

Enhanced Vitals Monitoring

"For participants in the intervention group, they will receive the enhanced continuous vital sign monitoring, on top of the standard of care monitoring as prescribed per the care team. The enhanced monitoring will be provided during the entire time period of hospitalization (up to 30 days after surgery), using the Philips monitor (i.e. heart rate and oxygen saturation continuously and blood pressure once an hour while awake). Participants and caregivers will be educated how to put on and off the devices by the study coordinator.~When participants return home, they will perform thrice-daily monitoring using the Cloud DX Inc. Home kit and daily questionnaires at home 7 days after discharge (or 30 days after surgery, whichever occurs first)."

Trial Locations (1)

V6Z 1Y6

St. Paul's Hospital, Vancouver

Sponsors
All Listed Sponsors
collaborator

Medtronic

INDUSTRY

collaborator

Providence Health Care Ventures

UNKNOWN

collaborator

Cloud DX Inc.

INDUSTRY

collaborator

Excelar

UNKNOWN

collaborator

3D Bridge Solutions

UNKNOWN

collaborator

Simon Fraser University

OTHER

collaborator

Providence Health & Services

OTHER

lead

University of British Columbia

OTHER