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临床试验/NCT00205192
NCT00205192已完成不适用

Optimizing Cardiac Resynchronization

University of Wisconsin, Madison1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2004年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
100
试验地点
1

研究概览

简要总结

Cardiac resynchronization therapy shows great promise as a method to improve ventricular function in heart failure due to dilated cardiomyopathy. It is applied to patients with class III and IV symptomatic heart failure on optimal therapy. Typical entry criteria in the trials testing resynchronization have used the electrocardiogram and a prolonged electrocardiogram (ECG) QRS interval as criteria for dyssynchrony. This is recognized to be quite limited as a tool for identifying patients. Several new echocardiographic methods for identifying dyssynchrony have been proposed. The purpose of this study is to systematically examine these multiple echocardiographic measurement techniques in three conditions:

  1. in the patient's native rhythm simulated by changing the pacing system to atrial pacing only;
  2. in conventional dual chamber pacing (DDD mode); and
  3. during biventricular pacing. All patients entered into this study will already have had a biventricular pacemaker placed.

研究设计

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

入排标准

性别
All
接受健康志愿者
否

入选标准

  • •All patients who have previously had a resynchronization pacemaker system placed at the University of Wisconsin Hospital or at the Middleton Veterans Hospital are potentially eligible for this study.
  • •The study is only open to patients as enumerated above, and also patients who have good imaging windows.

排除标准

  • 未提供

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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