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临床试验/EUCTR2011-001141-32-NL
EUCTR2011-001141-32-NL进行中(未招募)不适用

Catheter ablation versus Amiodarone to pRevent Future ventricular tachycardia Episodes in patients with a defibrillator and a history of a myocardial infarction - CARFE 2

Isala klinieken department Cardiology0 个研究点开始时间: 2011年4月27日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1.prior myocardial infarction, at least 3 months ago
  • 2.ICD implantation for any cause except for: Brugada syndrome, ARVC, HCM, LQTS, SQTS, cathecholaminergic polymorphic VT, other channelopathies
  • 3.ICD therapy (shock or ATP) for VT or VF without a reversible cause
  • 4.Optimal revascularization before ICD implantation performed
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1.Age < 18 years
  • 2.use of amiodarone more than 7 days before randomization within the period of 3 months before randomization
  • 3.Inability to use amiodarone due to past side effects
  • 4.Class I antiarrythmic drugs not stopped = 5 times ½T prior to randomization
  • 5.Protruding LV thrombus or cardiac tumor on pre-ablation echocardiogram
  • 6.Acute myocardial infarction within the preceding 3 months
  • 7.non-reversible Class IV NYHA heart failure
  • 8.Valvular heart disease or mechanical heart valve precluding access to the left ventricle.
  • 9.Unstable coronary artery syndrome or active myocardial infarction
  • 10.Cardiac surgery within the past 2 months
  • 11.mechanical mitral or tricuspid valve prothesis
  • 12.Serum creatinine > 220 mmol/L (2.5 mg/dL)
  • 13.Thrombocytopenia or coagulopathy
  • 14.Contraindication to anticoagulation
  • 15.stroke within past 30 days
  • 16.Pregnancy

研究者

发起方
Isala klinieken department Cardiology

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