DRKS00034194招募中不适用
Investigation of the genetic basis of unexplained monogenic diseases - Genom4ME
Institut für Humangenetik und Genommedizin der Uniklinik RWTH Aachen0 个研究点目标入组 3,000 人开始时间: 2024年5月8日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 3,000
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
- one 至 one（—）
- 性别
- All
入选标准
- •Suspicion of monogenic disease, consent available
排除标准
- •Lack of consent
研究者
相似试验
招募中
不适用
Elucidating the genetic pathomechanism underlying rare and hereditary kidney diseasesChronic kidney diseaseDRKS00008910Institut für HumangenetikUniklinik Köln3,000
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
已完成
不适用
Identification of the genetic pathways involved in patients overreacting to radiotherapyNL-OMON35606MAASTRO clinic6
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
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