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临床试验/ISRCTN62488166
ISRCTN62488166已完成不适用

Substrate Mapping and Ablation in Sinus rhythm to Halt Ventricular Tachycardia

Beth Israel - Deaconess Hospital (USA)0 个研究点目标入组 128 人开始时间: 2006年9月25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
128

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • Men and women who were at least 18 years old were eligible for the study if they had a history of an MI as documented by an electrocardiogram or cardiac imaging and had a planned or recent (within six months) implantation of an ICD for either:
  • 1. Ventricular Fibrillation (VF) arrest
  • 2. Hemodynamically-unstable Ventricular Tachycardia (VT)
  • 3. Syncope and inducible VT during invasive electrophysiologic testing (for this group, syncope is assumed to be the qualifying spontaneous arrhythmic event)
  • 4. Patients who had received an ICD for primary prophylaxis and then experienced a single appropriate ICD therapy

排除标准

  • 1. Treated with a Class I/III antiarrhythmic drug
  • 2. The substrate for the ventricular arrhythmia was thought not to be due to the myocardial infarction
  • 3. Active ongoing cardiac ischemia was felt to be the cause of the ventricular arrhythmia;
  • 4. Incessant or multiple VT episodes necessitating some form of treatment ? drugs or ablation
  • 5. Unable to give informed consent
  • 6. If the patient had experienced a stroke within 30 days
  • 7. Contraindication to anticoagulation
  • 8. Any medical/non-medical condition likely to prevent completion of the trial

研究者

发起方
Beth Israel - Deaconess Hospital (USA)

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