NL-OMON37798
已完成
不适用
Molecular genetics of familial heart disease - Genetics of familial heart disease
概览
- 阶段
- 不适用
- 干预措施
- 未指定
- 疾病 / 适应症
- congenital heart defect
- 发起方
- Academisch Medisch Centrum
- 入组人数
- 300
- 状态
- 已完成
- 最后更新
- 去年
概览
简要总结
暂无简介。
研究者
入排标准
入选标准
- •Individuals from families with two or more affected persons with congenital heart disease and/or (thoracic) aortic aneurysm are included. Affected family members as well as unaffected family members are included.
排除标准
- 未提供
结局指标
主要结局
未指定
相似试验
已完成
不适用
Signs and Symptoms Associated With Molecular Defects in Genetically Inherited Heart DiseaseCongenital Heart DefectNCT00027196National Heart, Lung, and Blood Institute (NHLBI)9,999,999
已完成
不适用
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart DiseaseCardiomyopathy, Hypertrophic, FamilialNCT00001881National Heart, Lung, and Blood Institute (NHLBI)9,999
招募中
不适用
Genetic Origin of Congenital Heart Disease Identification of genetic variants causing congenital heart diseaseCongenital Heart DiseaseHeart Defects10010394NL-OMON47377niversitair Medisch Centrum Utrecht1,050
已完成
不适用
Family Heart Study (FHS)Cardiovascular DiseasesAtherosclerosisCoronary DiseaseHeart DiseasesNCT00005136University of Minnesota
招募中
不适用
The Electronic Cardiovascular Genetics (eCG) Clinic for Presymptomatic Genetic CounsellingInherited Cardiac DiseaseNCT06431425UMC Utrecht170