跳至主要内容
临床试验/NCT01696136
NCT01696136已完成不适用

Multi-electrode PulmonarY Vein Isolation Versus Single Tip Wide Area Catheter Ablation for PAF a Randomized Multinational Multicenter Trial

L.V.A. Boersma2 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2011年1月1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
120
试验地点
2
主要终点
Freedom of AF

研究概览

简要总结

The MYSTIC_PAF trial investigates the differences between treatment with a single-tip catheter against a multielectrode catheter in cardiac ablation procedures in patients with paroxysmal atrial fibrillation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • History of symptomatic paroxysmal atrial fibrillation defined as:
  • Self-terminating AF with episodes lasting no more than seven consecutive days before spontaneous conversion back to sinus rhythm
  • Documentation of one or more events with PAF tracings by ECG, event recordings, pacemaker strips or monitor rhythm strips within the past year
  • AF symptoms defined as the manifestation of any of the following:
  • Palpitations
  • Exertional dyspnea
  • Effort intolerance
  • Age between 18 and 70
  • Willingness, ability and commitment to participate in baseline and follow-up evaluations for the full length of the study

排除标准

  • Structural heart disease of clinical significance including:
  • Previous cardiac surgery (excluding CABG)
  • Symptoms of congestive heart failure including, but not limited to, NYHA Class III or IV CHF and/or documented ejection fraction < 40% measured by acceptable cardiac testing
  • Left atrial diameter of > 50mm as measured in the parasternal long axis on transthoracic echocardiogram
  • Stable/unstable angina or ongoing myocardial ischemia
  • Myocardial infarction (MI) within three months of enrollment
  • Aortic or mitral valve disease > Grade II
  • Congenital heart disease (not including ASD or PFO without a right to left shunt) where the underlying abnormality increases the risk of an ablative procedure
  • Prior ASD or PFO closure with a device using a percutaneous approach
  • Hypertrophic cardiomyopathy (LV wall thickness > 1.5 cm)
  • Pulmonary hypertension (mean or systolic PA pressure >50mm Hg on Doppler echo
  • Prior ablation for arrhythmias other than AF within the past three months
  • Prior left sided AF ablation
  • Enrollment in any other ongoing arrhythmia study protocol Any ventricular tachyarrhythmias currently being treated where the arrhythmia or the management may interfere with this study

结局指标

主要结局

Freedom of AF

时间窗: Month 3 after intervention

Is the patient free of Atrial Fibrillation, at month 3 after the ablation intervention, and not taking anti-arrhythmic drugs

次要结局

未报告次要终点

研究者

发起方
L.V.A. Boersma
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

L.V.A. Boersma

Cardiologist

R&D Cardiologie

研究点 (2)

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