NCT01792960已完成不适用
Registry and Prevalence of Gene Mutation in Korean Patients With Familial Hypertrophic Cardiomyopathy
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 99
- 试验地点
- 1
- 主要终点
- 1) DNA analysis
研究概览
简要总结
Set the Korean Familial Hypertrophic Cardiomyopathy (KFHC) registry to study the prevalence of gene mutations in Korean patients with familial hypertrophic cardiomyopathy
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
- 13 Years 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •left ventricular maximal wall thickness ≥ 15mm on echocardiography
- •hypertrophic cardiomyopathy patients' relatives
排除标准
- •other cardiomyopathy or systemic disease (e.g. fabry disease, danon disease, glycogen storage disease)
- •who deny the study entrance, especially in patients' relatives
结局指标
主要结局
1) DNA analysis
时间窗: 1 year
1) Identify susceptible genes for familial hypertrophic cardiomyopathy in Korean
次要结局
- 2) Prognosis of familial hypertrophic cariomyopathy(1 year)
研究者
研究点 (1)
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