JPRN-UMIN000023100已完成未知
The Single-center Prospective Randomized Controlled Trial Evaluating Efficacy and Safety of Catheter Ablation without Periprocedual Contrast Media for Paroxysmal Atrial Fibrillation: Sophisticated Atrial Fibrillation ablation procedurE contrasT media unnecessitY (SAFETY) trial - SAFETY trial
Kyoto University Graduate School of Medicine,0 个研究点目标入组 100 人开始时间: 2016年9月10日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 100
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
- 20years-old 至 80years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1)Patients with a history of allergy for contrast media 2)Patients with renal insufficiency (eGFR <=45ml/min/1.73m2 3)Left ventricular ejection fraction < 40% 4)Left atrial diameter > 50mm 5)Patients with a history of open heart surgery 6)Patients with moderate or severe valve heart disease 7)Patients who need additional ablation such as tricuspid valve isthmus ablation during procedure 8)Patients unwilling to sign the consent form for participation
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