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临床试验/ISRCTN11980212
ISRCTN11980212已完成未知

Assessment of genetic predisposition to development of primary ventricular fibrillation in patients with acute myocardial infarction

niversità degli Studi di Pavia0 个研究点目标入组 4,000 人开始时间: 2016年12月29日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
4,000

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

性别
All

入选标准

  • 1. Age between 18 and 75 years, inclusive
  • 2. At least one episode of cardiac arrest due to ventricular fibrillation within 24 h of onset of symptoms of heart attack documented in the index electrocardiogram
  • 1. Age between 18 and 75 years, inclusive
  • 2. Episode of myocardial infarction within 24 h of onset of symptoms

排除标准

  • Case Patients
  • 1. Age younger than 18 or older than 75 years
  • 2. History of previous myocardial infarction
  • 3. Pre-existing significant cardiac disease and / or associated with Ejection Fraction less than or equal to 30%
  • 4. Presence of arrhythmogenic diseases that affect the occurrence of major ventricular arrhythmias (TV, FV) independently by the ischemic event (arrhythmogenic right end/or left ventricular cardiomiopathies, long- and short-QT syndrome; Brugada syndrome and Cathecolaminergic polymorphic ventricular tachicardia)
  • Control Patients
  • 1. Age younger than 18 or older than 75 years
  • 2. History of previous myocardial infarction
  • 3. Pre-existing significant cardiac disease and / or associated with Ejection Fraction less than or equal to 30%
  • 4. Presence of arrhythmogenic diseases that affect the occurrence of major ventricular arrhythmias (TV, FV) independently by the ischemic event (arrhythmogenic right end/or left ventricular cardiomiopathies, long- and short-QT syndrome; Brugada syndrome and Cathecolaminergic polymorphic ventricular tachicardia)

研究者

发起方
niversità degli Studi di Pavia

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