NCT04460209已完成不适用
EP Device Registry
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 5,003
- 试验地点
- 26
- 主要终点
- The proportion of patients with a device- and/or procedure-related Serious Adverse Event
研究概览
简要总结
This study will provide ongoing, high quality data on the safety, performance, and clinical benefits of Abbott's EP devices in a real-world setting.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Subject underwent an electrophysiology imaging (diagnostic procedure) and/or ablation procedure that used one or more Abbott devices covered by this Registry.
- •Subject is willing and able to comply with the site's standard of care follow-up schedule.
排除标准
- •Subject is currently participating in another clinical investigation that may confound the results of this Registry.
结局指标
主要结局
The proportion of patients with a device- and/or procedure-related Serious Adverse Event
时间窗: 7-days
that occurred within 7-days of the procedure.
The proportion of procedures that achieved acute success.
时间窗: Baseline
次要结局
未报告次要终点
研究者
研究点 (26)
Loading locations...
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