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
| Type | Name | Description |
|---|---|---|
| DEVICE | Cardiac monitoring device | Portable, 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.