None listed
Conditions
Interventions
Medical Device : 1) Active Comparator: Conventional Holter Monitoring Group
Holter monitoring is performed for 24 hours each at 1, 3, and 12 months after the diagnosis of stroke, and if atrial fibrill
Sponsors
Ewha Womans University Medical Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: All patients, except those with atrial fibrillation, who first came to our neurology department after IRB approval for stroke or transient ischemic attack.
Exclusion criteria
Exclusion criteria: - Excluding patients who have previously had atrial fibrillation or whose atrial fibrillation was first detected on the first surface electrocardiogram - Excluding patients who cannot use the Kardia Mobile system by themselves or with the help of others. - Excludes patients with artificial pacemakers (pacemakers), implantable defibrillators, or other implantable electrical devices. - Excluding pregnant women and lactating women. - Excluding cases with current symptoms or history of skin cancer, rash, skin disease, keloid or injury.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Compare atrial fibrillation detection rates of each arms | — |
Secondary
| Measure | Time frame |
|---|---|
| Major adverse cardiovascular and cerebrovascular event;Change from antiplatelet therapy to anticoagulants following AF detection;Major bleeding;Re-admission;All-cause death | — |
Countries
Korea, Republic of
Contacts
Public ContactSoomi Jung
Ewha Womans University Medical Center
Outcome results
None listed