跳至主要内容
临床试验/NCT01114035
NCT01114035已完成不适用

Characterization Phenotypic and Genetic Study of the Intestinal Epithelial Dysplasia or TE

Assistance Publique - Hôpitaux de Paris2 个研究点 分布在 1 个国家目标入组 41 人开始时间: 2010年4月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
41
试验地点
2
主要终点
gene identification

研究概览

简要总结

This PHRC is centred on the intestinal epithelial dysplasia ( DEI) or " tufting enteropathy " or TE the clinical and histo-pathological descriptions of which are specified well to the digestive plan(shot).

详细描述

The objectives of this PHRC are:

  • the phenotypic analysis of the intestinal epithelial dysplasia by clinical and histo-pathological investigations.
  • the identification of proteins involved at the intestinal level in the differentiation, the proliferation and the membership of the epithelial cells
  • from the phenotypic study, a genetic analysis of type maps by homozygote on the whole genome partner in an approach guided by possible candidate genes
  • the study of the genes, chosen according to their location, to their profile of expression, and to their function in touch with the pathogenic hypotheses

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
— 至 15 Years(Child)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

gene identification

时间窗: 6 months

identification of different family of genes involved in intestinal dysplasia

次要结局

  • mutation identification(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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