JPRN-UMIN000045447招募中未知
Retrospective study about the prognosis in patients with non-valvular atrial fibrillation who underwent a percutaneous left atrial appendage closure. - Retrospective study about left atrial appendage closure device
Department of Cardiology, Kokura Memorial Hospital0 个研究点目标入组 100 人开始时间: 2021年9月10日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 100years-old(—)
- 性别
- All
入选标准
- 未提供
排除标准
- •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.
研究者
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