jRCTs032180018已完成不适用
Randomized crossover trial comparing a wearable 2-week ECG versus standard 24-hour ECG to detect a recurrence of atrial fibrillation after the catheter ablation (hitoe-2)
未提供0 个研究点目标入组 70 人开始时间: 2018年10月24日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 70
- 主要终点
- -
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized Controlled Trial
- 干预模型
- Crossover Assignment
- 主要目的
- Diagnostic Purpose
- 盲法
- Open(masking Not Used)
入排标准
- 年龄范围
- 20age old over 至 No limit（—）
- 性别
- All
入选标准
- •Patients who underwent an initial catheter ablation for atrial fibrillation
排除标准
- •Allergies
- •Very sensitive skin to adhesive tape with a history of redness, erosion and scar
- •Cardiac implantable electronic devices
结局指标
主要结局
-
Detection of recurrent atrial fibrillation
次要结局
未报告次要终点
研究者
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