Two ways to catch a hidden heart rhythm after stroke
NCT ID NCT05822791
First seen Sep 18, 2026 · Last updated Sep 18, 2026
Summary
Researchers are comparing two ways of finding atrial fibrillation in people who have had an ischemic stroke or a transient ischemic attack (TIA). One method uses a standard electrocardiogram (ECG) in the hospital, and the other uses a prolonged cardiac monitor worn for a longer period. The study reviews records from 366 patients in the London Ontario Stroke Registry to see whether the two detection methods are linked to different rates of recurrent stroke, death, or hospital readmission for heart problems.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If the two detection methods identify different risks, doctors could tailor how closely they watch stroke survivors for recurring atrial fibrillation and future strokes.
- What could go wrong
- This is a single-center review of past records, so it can show patterns but cannot prove that one monitoring method causes better outcomes. The findings may not apply to other hospitals or patient groups.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 366 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2023
- Expected to finish
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Oct 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with an acute ischemic stroke or TIA in the London Ontario Stroke Registry without known AF, who are newly diagnosed with AF on a 12-lead ECG or a ≥7-day external cardiac monitor.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Heart & Brain Lab, Western University
London, Ontario, N6A 5A5, Canada
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