Retrospective study about the prognosis in patients with non-valvular atrial fibrillation who underwent a percutaneous left atrial appendage closure.

Not Applicable

Recruiting

• Conditions: onvalvular atrial fibrillation

• Registration Number: JPRN-UMIN000045447
• Lead Sponsor: Department of Cardiology, Kokura Memorial Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-09-10
• Last Update Posted: 17 October 2023
• Study Completion: 2031-09-02

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

Not provided

Exclusion Criteria

1. patients requiring long-term use of oral anticoagulants for reasons other than non-valvular atrial fibrillation (e.g., patients with implanted mechanical prosthetic valves, patients with hypercoagulable states, or patients with recurrent DVT) 2. patients with evidence of intracardiac (especially intra-atrial) thrombus. 3. patients with atrial septal defect or foramen ovale repair (surgery, device implantation, etc.), or patients with atrial septal defect or foramen ovale repair (surgery, device implantation, etc.). Patients with a history of atrial septal defect or atrial septal suture closure. 4. patients with anatomical structures of the left ventricular ear that are not amenable to closure devices. 5. patients with contraindications to left ventricular closure (transesophageal echocardiography (TEE)) or patients with contraindications to left ventricular closure (e.g., difficulty in inserting transesophageal echocardiography (TEE) probe or catheter required for the procedure). 6. patients with contraindications to anticoagulation, aspirin, or thienopyridine.

Study & Design

• Study Type: Interventional
• Study Design: Not specified