ISRCTN91372291已完成不适用
Post-market clinical follow-up study evaluating the efficacy and safety of LifeVest in real-life settings in France
ZO0 个研究点目标入组 550 人开始时间: 2016年1月29日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 550
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 性别
- All
入选标准
- •Patients receiving a LifeVest prescription in clinical routine. The following indications are authority approved:
- •1. Implantable cardiac defibrillator (ICD) removal due to cardiac device infections
- •2. A bridge to heart transplantation
- •3. In the early post-MI period with left ventricular (LV) dysfunction (LVEF <30%)
- •4. Recent coronary revascularization with LV dysfunction (LVEF < 30%)
排除标准
- •Patients who are physically or mentally unable to handle and use the WCD device appropriately, as judged by their responsible physician.
研究者
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