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Wearable Single-Lead Electrocardiogram Patch for detection of atrial fibrillation after an embolic stroke of undetermined origin: a multicenter randomized controlled trial

Not Applicable
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
Inclusion Criteria

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

Exclusion Criteria

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
NameTimeMethod
Diagnosis of Atrial Fibrillation
Secondary Outcome Measures
NameTimeMethod
Prescription of Anticoagulants
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