Patients with atrial fibrillation undergoing cardioversion will be randomized to undergo transesophageal echocardiography or they will receive warfarin for 3 weeks with an international normalized ratio (INR) value between 2.0-3.0. Those who do not want to use warfarin will be given an approved new oral anticoagulant agent instead of warfarin for 3 weeks. If thrombus is detected in left atrium or in left atrial appendage, no cardioversion will be performed. Other patients in the both groups will undergo electrical cardioversion. After the procedures all the patients will be given oral anticoagulant for at least 4 Weeks. All patients will have neurological examination and diffusion magnetic resonance imaging (MRI) at baseline and at postprocedural 7th day. Clinical and subclinical cerebral thromboembolic events detected by diffusion MRI will be recorded. Any bleeding events will also be recorded.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Combined Clinical Thromboembolic or Hemorrhagic Event, Death or Silent Cerebral Thromboemboli
Timeframe: 2 years
Efficacy Clinical End-point
Timeframe: 2 years
Ischemic Stroke/Transient Ischemic Attack
Timeframe: 2 years
Acute Ischemia in MRI
Timeframe: 1 week
Mortality
Timeframe: 2 years
Hemorrhagic Stroke
Timeframe: 2 years
Gastrointestinal Bleeding
Timeframe: 2 years