NL-OMON38774已完成不适用
Reveal LINQ Usability Study - Reveal LINQ
Medtronic Trading NL BV0 个研究点目标入组 50 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 50
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
- 18 至 99（—）
入选标准
- •Subject is indicated for a Reveal device
- •o Phase I (initial 30 subjects): Any indication for a Reveal LINQ Device
- •o Phase II (after the initial 30 subjects): Subject has atrial fibrillation and is
- •indicated for and identified as an AF pre-ablation candidate
排除标准
- •* Subject has an active implanted cardiac medical device (e.g., IPG, ICD, CRT).
- •* Subject is unwilling or unable to comply with the study procedures
研究者
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