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临床试验/KCT0008764
KCT0008764尚未招募Unknown

Efficacy and safety of catheter-based biatrial linear ablation for very long-standing persistent atrial fibrillation: a prospective observational registry

Asan Medical Center0 个研究点目标入组 69 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
尚未招募
入组人数
69

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
19(Year) 至 85(Year)(—)
性别
All

入选标准

  • Adults aged between 18-85
  • Diagnosed with persistent atrial fibrillation lasting for more than 7 days, as confirmed by a 12-lead ECG, Holter monitor, event recorder, or exercise stress test
  • Patients who have been diagnosed with atrial fibrillation for more than 3 years but less than 10 years
  • Resistant to or having side effects from one or more class I or III antiarrhythmic drugs
  • Patients receiving their first (de-novo) catheter ablation procedure for atrial fibrillation

排除标准

  • Refusal to participate in the research
  • BMI = 35kg/m^2
  • Intracardiac thrombus
  • Contraindications to anticoagulant therapy
  • History of surgical or interventional treatment for atrial fibrillation
  • Severe valvular heart disease, aortic stenosis, or mechanical prosthetic valve
  • Anteroposterior diameter of the left atrium of 60mm or more
  • NYHA class IV heart failure
  • Thoracic surgery within the last 3 months
  • Planned thoracic surgery within the next 3 months
  • End-stage heart failure or severe renal failure (estimated glomerular filtration rate [MDRD method] < 30mL/min/1.73m)
  • Pregnant or breastfeeding women
  • Acute coronary syndrome within the last 3 months
  • Co-morbidity (such as ongoing cancer treatment) with expected survival of less than 1 year

研究者

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