Heart Monitoring Device After Acute Myocardium Infarction
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 358
- 主要终点
- Heart rhythm monitoring
研究概览
简要总结
Verify the effectiveness of a Heart Monitor in preventing events in patients over 18 years after acute myocardial infarction in a clinical unit. Patients with neurological disease or congenital heart disease we excluded from the study.
详细描述
Heart Monitor can detect early intercurrences. Objective: To verify the effectiveness of a Heart Monitoring system in preventing events in patients after acute myocardial infarction. Methodology: This is a randomized clinical trial to be developed in a clinical unit and will include patients over 18 years , post-acute myocardial infarction who were transferred from the ICU emergency or hemodynamic to clinical unit. Patients with neurological disease or congenital heart disease will be excluded from the study.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- None
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 over 18 years
- •patients post-acute myocardial infarctium
排除标准
- •patients with neurological disease
- •patients with congenital heart disease
研究组 & 干预措施
Heart Monitor
We used the device (heart monitor) in the patients with myocardial infarction.
干预措施: Heart monitor (Device)
No Heart Monitor
No heart monitor device in the patients with myocardial infarction (control).
干预措施: No heart monitor (Device)
结局指标
主要结局
Heart rhythm monitoring
时间窗: One year
Evaluating the effectiveness of a heart monitoring device in the prevention and detection of events in patients after acute myocardial infarction
次要结局
未报告次要终点