Safety and Efficacy of Left Atrial Ablation After Percutaneous Left Atrial Appendage Occlusion in High-Bleeding-Risk Patients With Atrial Fibrillation: PROCEED-AF Ablation Registry
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 198
- 试验地点
- 20
- 主要终点
- Patient characteristics
研究概览
简要总结
The purpose of this multicenter study is to collect information from routine clinical practices for patients with left atrial appendage occlusion (LAAO) devices presenting for pulmonary vein isolation (PVI) or left atrial ablation. Assessment will include characterization of patient characteristics, procedural details, management of post-procedure anticoagulation, and clinical outcomes.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Individuals aged >18 years
- •Undergoing any type of atrial fibrillation ablation or left atrial arrhythmia ablation
排除标准
- •Missing essential baseline characteristics and/or missing collection of sufficient details regarding each complication
研究组 & 干预措施
Individuals undergoing atrial ablation for routine care
Individuals undergoing any type of atrial fibrillation ablation or left atrial arrhythmia ablation for routine care
干预措施: Data collection (Other)
结局指标
主要结局
Patient characteristics
时间窗: Month 0, baseline
Data will be collected to characterize patients with left atrial appendage occlusion devices presenting for pulmonary vein isolation or left atrial ablation
Procedural characteristics
时间窗: Month 0, during procedure
Data will be collected to characterize pulmonary vein isolation or left atrial ablation procedural details for patients with left atrial appendage occlusion devices
Post-procedure anticoagulation management
时间窗: Through 24 months
Data will be collected to characterize post-procedure anticoagulation management for patients with left atrial appendage occlusion devices
Clinical outcomes
时间窗: Through 24 months
Data will be collected to characterize clinical outcomes for patients with left atrial appendage occlusion devices presenting for pulmonary vein isolation or left atrial ablation
次要结局
- Procedure-related complications(Through 6 months)