Actively Recruiting
CARE-AF: Cardiac Assessment for Recurrent Stroke Risk Evaluation in Atrial Fibrillation
Led by Insel Gruppe AG, University Hospital Bern · Updated on 2025-11-20
500
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying patients with atrial fibrillation (AF), a common heart rhythm disorder, to better understand why some still experience ischemic strokes despite taking oral anticoagulant therapy (OAC). The study focuses on identifying clinical factors, cardiac serum biomarkers, and heart structure features that may be linked to breakthrough strokes and could improve risk prediction in high-risk AF patients. This observational study is conducted at a single center and aims to include at least 500 participants. Participants with AF who have had an acute ischemic stroke will be enrolled, including those with breakthrough strokes despite OAC use. The study does not involve any intervention but collects detailed clinical data, blood samples for cardiac biomarkers, and echocardiographic measurements of the left atrium and its appendage. Patients will undergo standardized follow-up visits every 12 months after enrollment, with a minimum follow-up period of 12 months. During the study, researchers will assess recurrent ischemic stroke or systemic embolism as the primary outcome, measured at the first follow-up around 12 months and annually thereafter. Secondary outcomes include all-cause death, major adverse cardiac events, episodes of symptomatic AF, and functional outcomes such as disability and quality of life. The study aims to enhance understanding of stroke risk factors in AF patients to guide future treatment decisions and improve risk stratification.
CONDITIONS
Brief Title
Cardiac Assessment for Recurrent Stroke Risk Evaluation in Atrial Fibrillation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 218 years or older
- Written informed consent by patient, next of kin, or legally authorized representative
- Diagnosed with permanent, persistent, or paroxysmal atrial fibrillation before or during the index hospital stay
- Acute symptomatic ischemic stroke within 7 days
You will not qualify if you...
- Life expectancy less than 1 year as judged by the investigator
- Unlikely to attend follow-up visits
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - At least 12 months
Participants are monitored over time to assess recurrent stroke risk and other cardiovascular outcomes.
Follow-up visits every 12 months
Trial Site Locations
Total: 1 location
1
Inselspital Bern
Bern, Switzerland, 3010
Actively Recruiting
Research Team
D
David Seiffge, Prof. MD
E
Elias Auer, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here