Atrial Fibrillation Clinical Trials

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Evolution of Burden of AF Biomarkers, Left Atrial Characteristics, Demographics,and Risk Factors in AF Detected After Stroke

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Adult patients with cortical or subcortical, cryptogenic or non-cryptogenic acute ischemic stroke

• Any of the following types of AF:

• Paroxysmal AF known before stroke onset (KAF).

• Paroxysmal AF found on an admission or Emergency Department ECG (ECG-AFDAS)

• Paroxysmal AF found on 14-day Holter monitoring (PCM-AFDAS)

Locations
Other Locations
Canada
Heart and Brain Lab, Western University
RECRUITING
London
Contact Information
Primary
Diana Ayan, Pharm MSc
diana.ayan@lhsc.on.ca
519-685-8500
Backup
Jennifer Moussa
jennifer.moussa@lhsc.on.ca
519-685-8500
Time Frame
Start Date: 2025-10-16
Estimated Completion Date: 2027-10
Participants
Target number of participants: 24
Treatments
Experimental: Participants with AF Detected After Stroke
Participants with AF detected after stroke undergo implantation of an insertable cardiac monitor (loop recorder) for continuous cardiac rhythm monitoring to detect and characterize atrial fibrillation burden, biomarkers, and left atrial characteristics over time.
Related Therapeutic Areas
Sponsors
Leads: Luciano A. Sposato

This content was sourced from clinicaltrials.gov