NCT02873169已完成不适用
Interest of Implantable Cardioverter-defibrillator in Primary Prevention in Patient With Continuous Flow Left Ventricular Assist Device (CF-LVAD)
Rennes University Hospital20 个研究点 分布在 1 个国家目标入组 681 人开始时间: 2015年9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
- 681
- 试验地点
- 20
- 主要终点
- Occurrence of early VAs (<30 days post operatively) and late VAs (>30 days post operatively) in patient with CF-LVAD with or without ICD
研究概览
简要总结
Determination of risk factors of ventricular arrhythmias (VAs) after implantation of continuous flow left ventricular assist device in order to characterize which patient requires ICD implantation in primary prevention.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
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 above 18 years old
- •Patients with CF-LVAD with or without ICD
排除标准
- •Patients subject to major legal protection (safeguarding justice, guardianship, trusteeship), persons deprived of liberty
结局指标
主要结局
Occurrence of early VAs (<30 days post operatively) and late VAs (>30 days post operatively) in patient with CF-LVAD with or without ICD
时间窗: 30 days
Clinical, biological, hemodynamic and rhythmic data
次要结局
- Mortality in patients with CF-LVAD with or without VAs(30 days)
- Mortality in patients with CF-LVAD with or without ICD(30 days)
研究者
研究点 (20)
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