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DETECTion of PeriOperative Atrial Fibrillation After Noncardiac Surgery

NCT06519747 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 750

Last updated 2024-11-07

No results posted yet for this study

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.

Conditions

Interventions

DEVICE

Cardiac monitoring device

Portable, up to 14 days of monitoring

Sponsors & Collaborators

  • Population Health Research Institute

    lead OTHER

Principal Investigators

  • David Conen, MD, MPH · Population Health Research Institute

  • Michael K Wang, MD · Population Health Research Institute

Eligibility

Min Age
18 Years
Max Age
120 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-10-15
Primary Completion
2026-08-15
Completion
2026-12-31

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06519747 on ClinicalTrials.gov