跳至主要内容
临床试验/NCT07577544
NCT07577544尚未招募不适用

Safety, Efficacy and Mid-term Outcomes of Pulsed Field Ablation for Mitral Isthmus Ablation Through Epicardial Approach

Shanghai Zhongshan Hospital0 个研究点目标入组 30 人开始时间: 2026年5月15日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
30

研究概览

简要总结

Why This Study Is Important

  • Many patients with atrial fibrillation (AF) continue to experience abnormal heart rhythms even after receiving standard treatments.
  • Standard heat-based energy can be difficult to use in these areas because fast blood flow cools the tissue, and excessive heat may damage nearby structures like the right coronary artery.

Our Approach

  • Investigators are testing a newer technology called pulsed field ablation (PFA).
  • Unlike traditional methods, PFA uses ultra-short electrical pulses rather than heat to target heart cells specifically while protecting neighboring nerves and blood vessels.
  • This study focuses on applying this energy within the coronary sinus to help achieve a more complete and lasting electrical block for the mitral isthmus.

What To Expect

  • This study involves 30 participants who are already undergoing a catheter ablation procedure for atrial fibrillation.
  • The research team will monitor how successful the procedure is at immediately stopping the abnormal electrical signals.
  • Participants will have follow-up visits over six months to check for any returning heart rhythm issues and will receive a specialized heart scan (CTA) to ensure the nearby coronary arteries remain healthy

研究设计

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

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Symptomatic Atrial Fibrillation: participants must have a diagnosis of symptomatic paroxysmal or persistent atrial fibrillation.
  • Documentation: The arrhythmia must be documented by electrocardiogram or Holter monitoring.
  • Age Range: participants must be between 18 and 75 years of age.
  • Study Compliance: participants must be willing and able to comply with the post-procedural follow-up schedule.
  • Procedural Requirement: All patients must be candidates for linear ablation at the mitral isthmus (MI) and coronary sinus (CS) for substrate modification.

排除标准

  • Prior Cardiac Procedures: Patients with a history of prior heart surgery or Left Atrial Appendage Occlusion (LAAO) are excluded.
  • Heart Failure Severity: Individuals classified with New York Heart Association (NYHA) functional class III or IV are ineligible.
  • Renal Impairment: Patients with advanced renal failure, defined as an estimated glomerular filtration rate (eGFR) below 30 mL/min/1.73m², are excluded.
  • Intracardiac Thrombus: Any patient with a left atrial thrombus identified via transesophageal echocardiography (TEE) is excluded.

研究者

发起方
Shanghai Zhongshan Hospital
申办方类型
Other
责任方
Sponsor

相似试验