NL-OMON20548已完成Unknown
The contribution of genetic predisposition to pediatric cancer: a study integrating extensive phenotyping and state of the art genotyping
Princes Máxima Center for pediatric oncology0 个研究点目标入组 843 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 843
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
- 0 至 17(—)
入选标准
- •- Children (age < 19 years) newly diagnosed with cancer or neoplasms at the Princess Máxima Center - Written informed consent (by patient when aged 16 years or older, by patient and parent(s) when aged 12-16 years, by parent(s) when younger than 12 years)
排除标准
- •- Patients and/or their parents who don't want to know the results of the DNA test (pediatric cancer gene panel analysis)
研究者
相似试验
已完成
不适用
The contribution of genetic predisposition to pediatric cancer: a study integrating extensive phenotyping and state of the art genotyping.NL-OMON52506Prinses Máxima Centrum voor Kinderoncologie843
已完成
不适用
The impact of genetic predisposition in pediatric renal cancer: genotypic and phenotypic characterizatioNL-OMON46432Prinses Máxima Centrum voor Kinderoncologie120
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
Multi-Ethnic New Zealand Study of Acute Coronary SyndromesCardiovascular - Coronary heart diseaseHuman Genetics and Inherited Disorders - Other human genetics and inherited disordersAcute coronary syndromeACTRN12615000676516The University of Auckland3,000
