AI-Assisted Workflow for Occult Atrial Fibrillation Detection After Ischemic Stroke: A Prospective Randomized Trial
Sponsor: National Taiwan University Hospital
Trial Details
| Condition | Atrial Fibrillation, Stroke, Artificial Intelligence |
| Intervention | Active Follow-up Group; Standard Follow-up Group |
| Phase | NA |
| Status | Not_yet_recruiting |
| Participants | 400 |
| Est. Completion | 31 Dec 2028 |
| Last Updated | 20 Apr 2026 |
Primary Outcome
The difference betwee Active Group & Standard Group
Eligibility Criteria
Inclusion Criteria
Inclusion Criteria: 1. 18 years or older who are acutely hospitalized due to ischemic stroke; 2. A 12-lead electrocardiogram upon admission showing sinus rhythm; Exclusion Criteria: 1. Previous diagnosis of atrial fibrillation or flutter; 2. Diagnosis of atrial fibrillation during hospitalization; 3. Pre-existing cardiac implantable electronic device (IVD); 4. Expected inability to attend regular outpatient follow-ups after discharge, or to undergo multiple 14-day ECG recordings; 5. Requires long-term anticoagulant use for other reasons, including but not limited to chronic pulmonary embolism; 6. Known contraindications to non-vitamin K antagonist oral anticoagulants due to comorbidities, including but not limited to end-stage renal disease, severe mitral stenosis due to rheumatic heart disease, or metallic heart valves; 7. Unwilling to sign a participant consent form.
Trial Sites
Countries
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