NCT02075866Unknown不适用
Finnish Genetic Study for Arrhythmic Events
适应症
试验速览
- 阶段
- 不适用
- 入组人数
- 8,000
- 试验地点
- 1
- 主要终点
- sudden cardiac death
研究概览
简要总结
Finnish Genetic Study for Arrhythmic Events (FinGesture is a prospective case-control study assessing the characteristics and genetic background of consecutive series of autopsy verified out-of-hospital victims of SCD vs. survivors of an acute coronary event in a specific geographical area in northern Finland.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 时间视角
- Prospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Sudden cardiac death verified by medicolegal autopsy (cases)
- •Acute coronary event (increased troponin levels/ECG markers of ischemia/angina pectoris; two out of three criteria) (controls).
排除标准
- •Sudden death due to other causes (cases).
- •Acute coronary event patients who died during hospitalization (controls).
结局指标
主要结局
sudden cardiac death
时间窗: 20 years
次要结局
未报告次要终点
研究者
研究点 (1)
Loading locations...
相似试验
Unknown
不适用
Arrhythmia Genetics in the NEtherlandSMyocardial Infarction FirstVentricular FibrillationNCT03007199Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)2,000
进行中(未招募)
不适用
Scandinavian Multicenter Study to Advance Risk Stratification in Heart Disease- Ventricular ArrhythmiasVentricular ArrhythmiasImplantable Defibrillator UserBiological MarkersHeart DiseaseNCT02864771University Hospital, Akershus504
已完成
不适用
Cardiac Arrhythmias in GreenlandAutonomic NeuropathyAtrial FibrillationArrhythmiaNCT05200676Aalborg University Hospital200
已完成
不适用
Arrhythmogenic Right Ventricular Dysplasia/CardiomyopathyArrhythmogenic Right Ventricular DysplasiaCardiomyopathyNCT00999947Assistance Publique - Hôpitaux de Paris351
Unknown
不适用
Molecular Genetic Screening and Identification of Congenital Arrhythmogenic DiseasesLong QT SyndromeArrhythmogenic Right Ventricular DysplasiaHypertrophic CardiomyopathyNCT00221832Heidelberg University300
