NCT00291564已完成不适用
Ensure Cardiac Resynchronization Therapy Study
Medtronic Cardiac Rhythm and Heart Failure0 个研究点目标入组 430 人开始时间: 2004年5月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 430
研究概览
简要总结
The purpose of this study is to gather information on how doctors program particular settings on cardiac resynchronization therapy implantable cardiac defibrillators (CRT-Ds), to analyze how these settings affect the amount of cardiac resynchronization therapy (CRT) patients receive and to evaluate the therapy approach for converting abnormally fast heartbeats into normal heartbeats. There are no experimental devices or procedures involved in this study.
研究设计
- 研究类型
- Observational
- 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
- 否
入选标准
- •Patient is indicated for a Medtronic CRT-D system
- •Patient is willing to sign Permission for Access to and Use of Health Information form
- •Patient is willing and able to comply with follow-up visits through six months
排除标准
- •Patient has a life expectancy of less than 6 months
- •Patient is participating in any concurrent study that could confound the results for either study
研究者
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