Differences in ECG- vs. proLonged cardIac MonItor-DeTected Atrial Fibrillation in STROKE Patients (DELIMIT AF-STROKE)

NCT05822791 · tracked via the Priya Life Science Canada tracker

Sponsor

Luciano A. Sposato

Phase

Observational

Started

2023-05-01

Last updated

2026-09-18

Condition(s) studied

StrokeAtrial FibrillationTIA

Investigational drug(s) / intervention(s)

Prolonged cardiac monitoringECG

Prolonged cardiac monitoring: Prolonged cardiac monitoring

ECG: Electrocardiogram

Study summary

The present study is an investigator-initiated, single-center, retrospective study based on data from the London Ontario Stroke Registry (LOSR), aiming to compare the characteristics and outcomes of ECG-detected and Device-Detected atrial fibrillation in patients with ischemic stroke and transient ischemic attack.

Eligibility

Sex

ALL

Min age

18 Years

Max age

—

Healthy volunteers

Inclusion Criteria: * Age ≥18 years * Patient with a diagnosis of ischemic stroke or TIA. * ECG-diagnosed AF or PCM-detected AF post ischemic stroke or TIA Exclusion Criteria: * Individuals younger than18 years-old * Patients without IS or TIA diagnosis

Primary outcome measure(s)

Number of Participants with Recurrent Ischemic Stroke at End of available Follow-up Time — Duration of follow-up - minimum of 3 months after the first encounter with the stroke team
Documented recurrent ischemic stroke

Trial sites (1)

Facility	City	Region	Status
Heart & Brain Lab, Western University	London	Ontario

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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 NCT05822791 on ClinicalTrials.gov ↗ ← All trials in Canada