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临床试验/NCT05959798
NCT05959798已完成不适用

High Power Short Duration Ablation Compared to Moderate Power Long Duration Ablation for Pulmonary Vein Isolation: Safety and Acute Procedural Outcome

Deutsches Herzzentrum Muenchen1 个研究点 分布在 1 个国家目标入组 204 人开始时间: 2019年4月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
204
试验地点
1
主要终点
Number of reconnected pulmonary veins 20 minutes after ablation in comparison of both ablation groups

研究概览

简要总结

High Power Short Duration Ablation Compared to Moderate Power Long Duration Ablation for Pulmonary Vein Isolation: safety and acute procedural outcome

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • symptomatic, documented, drug-resistent paroxysmal atrial fibrillation
  • effective oral anticoagulation

排除标准

  • any prior left atrial ablation procedure
  • presence of left atrial thrombus
  • secondary atrial fibrillation due to electrolyte imbalance or thyroid disease
  • any prior oesophageal or gastric surgery

结局指标

主要结局

Number of reconnected pulmonary veins 20 minutes after ablation in comparison of both ablation groups

时间窗: Acute endpoint

次要结局

  • Time to first documented recurrence of atrial fibrillation after a 6-week blanking period.(12 months after ablation)

研究者

发起方
Deutsches Herzzentrum Muenchen
申办方类型
Other
责任方
Sponsor

研究点 (1)

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