NL-OMON30598尚未招募不适用
Pedigree research in families with Common Variable Immunodeficiency Disease. - CVID families
Jeroen Bosch Ziekenhuis0 个研究点目标入组 20 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
- 尚未招募
- 发起方
- 入组人数
- 20
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
- •*patients with CVID treated at the department of pediatrics of the Jeroen Bosch Hospital.
- •*genetic interesting relatives of the CVID patients, based on the family history and pedigree.
- •*relatives with suspicion of immunodeficiency based on clinical records.
排除标准
- •Illness or recent infection (<2 weeks prior to inclusion).
研究者
相似试验
尚未招募
不适用
Genotype-phenotype relation within families with various forms of hereditary hemochromatosisiron overload disease1001469910022958NL-OMON29963Academisch Medisch Centrum120
已完成
不适用
Molecular studies in a multigenerational family with gastro-esophageal reflux disease (GERD)GERDheartburn1001801810017977NL-OMON35981Academisch Medisch Centrum23
进行中(未招募)
不适用
Why are more children getting Type 1 Diabetes? Exploring the environmental triggers islet autoimmunity and type 1 diabetesMetabolic and Endocrine - DiabetesInflammatory and Immune System - Autoimmune diseasesType 1 diabetesACTRN12613000794707niversity of Adelaide1,510
招募中
不适用
Identification of germline mutations in familial and extremely early-onset urinary bladder cancerbladder papilloma10038364bladder cancerNL-OMON41769niversitair Medisch Centrum Sint Radboud585
已完成
不适用
The identification of genetic variants in pedigrees with a high genetic loading for alcohol dependence10037176alcohol dependenceAddictionNL-OMON40342Academisch Medisch Centrum280
