Actively Recruiting
B2AD-Risk AFDAS Evolution of Burden of AF
Led by Luciano A. Sposato · Updated on 2026-05-07
24
Participants Needed
1
Research Sites
102 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Each year, 7.8 million people worldwide experience an ischemic stroke, often caused by atrial fibrillation (AF). AF is a major contributor to severe, disabling, and deadly strokes. About 20% to 30% of ischemic stroke patients have AF before their stroke. Of the remaining 70% to 80% without known arrhythmias, up to 24% are newly diagnosed with AF after intensive cardiac monitoring, totaling 1.3 to 1.5 million new AF cases detected after stroke globally each year. Oral anticoagulants (OACs) can reduce stroke risk related to AF by 64% and lead to milder strokes with lower disability and mortality. Neurologists use cardiac monitoring to detect AF in stroke patients. This study focuses on patients who have had an ischemic stroke and are newly diagnosed with AF. The goal is to understand how AF progresses over time. The investigators will track changes in AF severity and frequency, monitor biomarkers related to heart health, assess the size and function of the left atrium, and observe new risk factors like hypertension. Patients will be grouped based on their AF diagnosis method: ECG, a portable device recording heart activity for less than 7 days, or one recording for 7 to 30 days. The investigators hypothesize that AF burden will increase, new risk factors will emerge, biomarkers will rise, and the left atrium will worsen over time. Participants will be followed for up to 24 months with regular assessments. The study aims to provide insights into AF progression in stroke patients, potentially improving treatments and prevention strategies.
CONDITIONS
Official Title
B2AD-Risk AFDAS Evolution of Burden of AF
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients with cortical or subcortical, cryptogenic or non-cryptogenic acute ischemic stroke
- Paroxysmal atrial fibrillation known before stroke onset
- Paroxysmal atrial fibrillation found on an admission or Emergency Department ECG
- Paroxysmal atrial fibrillation found on 14-day Holter monitoring
You will not qualify if you...
- Patients not willing to consent
- Permanent or persistent atrial fibrillation
- Allergy to iodinated contrast agents
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Heart and Brain Lab, Western University
London, Ontario, Canada, N6A 5A5
Actively Recruiting
Research Team
D
Diana Ayan, Pharm MSc
CONTACT
J
Jennifer Moussa
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
1
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