NCT00583089已完成不适用
Decompensation Detection Study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 699
- 主要终点
- Data collection and analysis.
研究概览
简要总结
To gather data and analyze decompensation events.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 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
- •Patients implanted with an approved Guidant CRT-D HF device programmed to CRT therapy in VDD or DDD mode.
- •Patients prescribed to the LATITUDE(R) system configured for at least weekly device interrogations and symptoms reporting.
- •Patients willing to use the LATITUDE(R) enabled weight scale.
排除标准
- •Patients that require adaptive rate pacing (rate-responsive modes).
- •Patients that have received routinely scheduled intravenous inotropic therapy as part of their drug regimen within the past 90 days.
结局指标
主要结局
Data collection and analysis.
时间窗: End of patient follow up.
次要结局
未报告次要终点
研究者
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