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Clinical Trials in Canada / NCT05171569
Active, not recruiting Not applicable

Post Discharge After Surgery Virtual Care With Remote Automated Monitoring Technology-3 Trial

NCT05171569 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2021-12-28
Last updated
2025-03-27

Condition(s) studied

Surgery

Investigational drug(s) / intervention(s)

Virtual care with remote automated monitoring (RAM)

Virtual care with remote automated monitoring (RAM): Use of Cloud Diagnostics connected health kit for at home monitoring with virtual clinical from nursing and perioperative physician team.

Study summary

The Post discharge after surgery Virtual Care with Remote Automated Monitoring technology (PVC-RAM)-3 Trial is a multicentre, parallel group, superiority, randomized controlled trial to determine the effect of virtual care with remote automated monitoring (RAM) technology compared to standard care on length of index hospital stay and use of acute hospital care (composite of hospital readmission and emergency department visit) after randomization, in adults who have undergone elective non cardiac surgery. Secondary outcomes at 30 days after randomization include: 1) hospital re-admission; 2) emergency department visit; 3) medication error detection;4) medication error correction; 5) surgical site infection; and 6) days in hospital. Additional secondary outcomes are pain of any severity, and moderate-to-severe pain assessed at 15 and 30 days after randomization. The investigators will also assess optimal management of long-term health by evaluating among patients with atherosclerotic disease and current smokers whether patients are taking classes of efficacious medications at 30 days.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. are ≥18 years of age; 2. are undergoing inpatient elective noncardiac surgery with an expected length of hospital stay ≤3 days after surgery; and 3. provide informed consent to participate. Exclusion Criteria: 1. are unable to communicate with research staff, complete study surveys, or undertake an interview using a tablet computer due to a language barrier or a cognitive, visual, or hearing impairment; or 2. reside in an area without cellular network coverage.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Hamilton General Hospital Hamilton Ontario
Juravinski Hospital Hamilton Ontario

More Population Health Research Institute trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05171569 on ClinicalTrials.gov ↗ ← All trials in Canada