STUDY TYPE: Prospective, national , multicenter, and observational study. OBJECTIVE: To assess the incidence of AF in patients with cryptogenic stroke who have implanted an AF detection device during a period of 2 years. DEVICE: Reveal XT 9529 (SQDM) SAMPLE SIZE AND STUDY DURATION: 100 patients enrolled which will be followed during a period of 2 years.
Observational study in patients with cryptogenic stroke (TOAST criteria) and with an implanted EKG loop recorder, with the primary objective of knowing the atrial fibrillation incidence in this population
Study Type
OBSERVATIONAL
Enrollment
100
Hospital Universitario Virgen de la Arrixaca
Murcia, Murcia, Spain
RECRUITINGHospital Clinico Universitario de Valencia
Valencia, Valencia, Spain
RECRUITINGFirst AF episode detected by the implantable loop recorder in patients that had a cryptogenic stroke. An AF episode will be considered an AF episode that lasts at least 2 minutes.
Time frame: Patients will be followed up during two years, regardless of reaching or not the primary endpoint.
All subsequent AF episodes detected by the ILR after primary outcome (AF burden)
Time frame: Patients will be followed up during two years
AF episodes detected by external monitoring
Time frame: Patients will be followed up during two years
Presence of stroke, recurrent TIA, or silent infarction in neuroimaging
Time frame: Patients will be followed up during two years
Changes in anticoagulant therapy
Time frame: Patients will be followed up during two years
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