Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06519747

DETECTion of PeriOperative Atrial Fibrillation After Noncardiac Surgery

Enhanced DETECTion of PeriOperative Atrial Fibrillation After Noncardiac Surgery with Continuous Electrocardiographic Monitoring

Status
Recruiting
Phase
Study type
Observational
Enrollment
750 (estimated)
Sponsor
Population Health Research Institute · Academic / Other
Sex
All
Age
18 Years – 120 Years
Healthy volunteers
Not accepted

Summary

This is a multicentre prospective cohort study where patients will receive up to 14 days of continuous ECG monitoring by wearing a portable monitoring device, starting within 72 hours after noncardiac surgery.

Detailed description

POAF commonly occurs after noncardiac surgery and is associated with adverse long-term outcomes. Despite this, patients with POAF are routinely being missed during clinical practice. Continuous ECG monitoring has the potential to enhance POAF detection and improve clinical care in affected patients. Based on this background, the DETECT-POAF study will determine the incidence of clinically important POAF in those receiving up to 14 days of continuous ECG monitoring within 35 days after noncardiac surgery.

Conditions

Interventions

TypeNameDescription
DEVICECardiac monitoring devicePortable, up to 14 days of monitoring

Timeline

Start date
2024-10-15
Primary completion
2026-08-15
Completion
2026-12-31
First posted
2024-07-25
Last updated
2024-11-07

Locations

6 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT06519747. Inclusion in this directory is not an endorsement.