NL-OMON39758已完成不适用
Study of the genetic causes of disorders of the aorta, arteries and cardiac valves - Aorta
niversitair Medisch Centrum Sint Radboud0 个研究点目标入组 500 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 500
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
- 年龄范围
- 2 至 99（—）
入选标准
- •Inclusion criteria
- •1. Patients and familymembers with thoracic aortic aneurysm and dissection
- •2. Patients and familymembers with Marfan syndrome and related conditions
- •3. Patients and familymembers with bicuspid aortic valve, specifically if associated with aortic aneurysm or history of sudden death or aortic dissection
- •4. Patients and family members with arterial aneurysms and/or valve abnormalities
- •No restriction for age or sex.
排除标准
- 未提供
研究者
相似试验
已完成
不适用
The role of genetic factors in the aetiology of achalasiaNL-OMON39386Academisch Medisch Centrum450
已完成
不适用
A study to improve our understanding of the genetic causes of swelling in babies before birthFetal oedema/hydrops with a focus on lymphatic related hydropsPregnancy and ChildbirthConditions involving the integument and temperature regulation of fetus and newbornISRCTN22076461St George’s University Hospitals NHS Foundation Trust60
尚未招募
不适用
Study on genetic factors in the pathogenesis of Inflammatory Bowel Disease: Gathering a matched control populatioCrohns disease1001796910003816Ulcerative ColitisNL-OMON30241Academisch Medisch Centrum3,000
已完成
不适用
Exploratory Study of Genetic Factors Related to the Inhibitory Effect of Tolvaptan on Increased Kidney Volume in Patients with Autosomal Dominant Polycystic Kidney DiseaseAutosomal Dominant Polycystic Kidney DiseaseJPRN-UMIN000031976Otsuka Pharmaceutical Co.,Ltd.890
招募中
不适用
Clinical and molecular genetic aspects of idiopathic epilepsiesseizures1002929910039911epilepsyNL-OMON35523Epilepsiecentrum Kempenhaeghe300