Condition: Surgery · Post Operative Complications · Quality of Recovery · Sponsor: University of British Columbia
The aim of this clinical trial is to examine the feasibility of an enhanced vital sign monitoring solution in-hospital and at-home. This study includes adult patients undergoing inpatient major vascular or abdominal surgery. Researchers will compare the enhanced vitals monitoring group to the standard of care group to see if it may change post-operative management and outcomes. The primary question it aims to answer is if enhanced monitoring of surgical patient vitals can increase the number of days at home alive in the first 30 days after surgery. Participants in the intervention group will test two vitals monitoring devices, one in the hospital and one at home. They will also be asked to complete several questionnaires and a follow up phone call.
This description comes directly from the study's public registry record.
Janny Ke, MD · 604-816-3339 · janny.ke@ubc.ca
Nicola Edwards, MHA · 604-816-3339 · nedwards@providencehealth.bc.ca
Always discuss trial participation with your own doctor first.
| Mount Saint Joseph's Hospital | Vancouver, British Columbia, Canada | Recruiting |
| St. Paul's Hospital | Vancouver, British Columbia, Canada | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06584825