跳至主要内容
临床试验/NCT04055961
NCT04055961招募中不适用

Atrial Fibrillation Ablation Registry Protocol Number: 3122-2016

Hoag Memorial Hospital Presbyterian1 个研究点 分布在 1 个国家目标入组 5,000 人开始时间: 2019年5月20日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
5,000
试验地点
1
主要终点
Unsuccessful treatment rate

研究概览

简要总结

The Atrial Fibrillation Ablation Registry (AFib Ablation Registry™) is designed to assess the prevalence, demographics, management, and outcomes of patients undergoing percutaneous catheter ablation procedures to treat atrial fibrillation (AF).

详细描述

The Atrial Fibrillation Ablation Registry (AFib Ablation Registry™) is designed to assess the prevalence, demographics, management, and outcomes of patients undergoing percutaneous catheter ablation procedures to treat atrial fibrillation (AF). Patient-level data will be submitted by participating hospitals on a quarterly basis to the American College of Cardiology Foundation's National Cardiovascular Data Registry (NCDR™). The primary aims of the AFib Ablation Registry are to optimize the outcomes and management of patients through the implementation of evidence-based guideline recommendations in clinical practice, facilitate efforts to improve the quality and safety for patients undergoing percutaneous catheter ablation procedures, investigate novel quality improvement methods and provide risk-adjusted assessment of patients for comparison with nationwide NCDR data. The secondary purpose of the AFib Ablation Registry is to serve as a rich source of clinical data to support assessments of short- and long-term safety, comparative and cost effectiveness research, and as a scalable data infrastructure for post market studies.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Other

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients
  • 18 years and older
  • Undergoing percutaneous catheter ablation procedures to treat atrial fibrillation

排除标准

  • 未提供

结局指标

主要结局

Unsuccessful treatment rate

时间窗: 1 year

measured by the number of repeated procedure

次要结局

  • Adverse Events(1 year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Colleen Balius

Clinical Data Coordinator

Hoag Memorial Hospital Presbyterian

研究点 (1)

Loading locations...

相似试验