跳至主要内容
临床试验/NCT00562757
NCT00562757Unknown不适用

The Harbinger ICD Patient (HIP) Study

Harbinger Medical, Inc.8 个研究点 分布在 4 个国家目标入组 320 人开始时间: 2003年9月最近更新:
适应症

试验速览

阶段
不适用
入组人数
320
试验地点
8
主要终点
Life Threatening Cardiac Event (death or annotated malignant ventricular arrhythmia detected by ICD and confirmed by cardiologist review)

研究概览

简要总结

The purpose of this study is to determine how well the device predicts susceptability to potentially lethal ventricular arrhythmias.

详细描述

Sudden cardiac death (SCD) accounts for half of all deaths from cardiovascular causes, with an annual incidence of 1 to 2 deaths per 1000 population. In the United States this translates to between 300,000 to more than 400,000 deaths annually. Results from numerous large, well designed clinical trials have demonstrated the efficacy of the implantable cardioverter-defibrillator (ICD) for improving survival in patients with ischemic heart disease. However, measures used to risk stratify patients, such as left ventricular ejection fraction do not adequately identify those patients who can most benefit from ICD therapy. As a result, many patients who currently receive an ICD do not use the device. In addition, many more patients who could benefit from ICD therapy are outside of current guidelines and do not have access to this life-saving therapy.

This prospective study was intended to determine how well the Harbinger Wedensky Modulation Index (WMI) technique risk stratifies patients into two groups: those needing antiarrhythmic therapy and those who do not need antiarrhythmic therapy.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

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

  • Post myocardial infarction patients receiving ICD therapy

排除标准

  • Patients unable to give consent
  • Pacemaker dependant patients
  • Pregnant women

结局指标

主要结局

Life Threatening Cardiac Event (death or annotated malignant ventricular arrhythmia detected by ICD and confirmed by cardiologist review)

时间窗: Up to two years

次要结局

未报告次要终点

研究者

申办方类型
Industry

研究点 (8)

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