Wearable Single-Lead Electrocardiogram Patch for detection of atrial fibrillation after an embolic stroke of undetermined origin: a multicenter randomized controlled trial
- Conditions
- Diseases of the circulatory system
- Registration Number
- KCT0007505
- Lead Sponsor
- Hallym University Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 400
A. Adult patients aged 55 years or older who were hospitalized for ischemic stroke from November 1, 2021 to December 31, 2024
B. Patients who visited the hospital within 7 days after symptom onset (First abnormal time)
C. Patients with embolic stroke (ESUS) of unknown cause for ischemic stroke (Trial of ORG 10172 in Acute Stroke Treatment) classification
A. Patients wearing less than 50% of wearable devices during the study period
B. Patients who are unable to understand or adhere to the study protocol or who lack the ability to express themselves
C. Patients who have difficulty in ECG patching due to skin reactions or allergies
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Diagnosis of Atrial Fibrillation
- Secondary Outcome Measures
Name Time Method Prescription of Anticoagulants