跳至主要内容
临床试验/NCT01065233
NCT01065233已完成不适用

Genetical Predisposition in Hepatocellular Carcinoma : Pangenomic Link Study During Alcoholic Cirrhosis

Nantes University Hospital4 个研究点 分布在 1 个国家目标入组 1,325 人开始时间: 2008年10月23日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,325
试验地点
4
主要终点
Existence of HCC and Pangenomic analysis of DNA polymorphism

研究概览

简要总结

Hepatocellular carcinoma (HCC) is a frequent complication of cirrhosis. Occurrence of HCC could be linked with multiple functional region of genome.

The determining of a genomic mapping of " single nucleotide polymorphisms " (SNPs) permit to perform some genetic link studies with pathologies without clear hereditary disposition.

In this study, the investigators will identify predictives genetic polymorphism of HCC.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
35 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 35 to 70 years old
  • Compensated cirrhosis or not
  • Caucasian origin of the parents
  • Patient with cirrhosis (histological proof or obvious)

排除标准

  • HIV, HBV, HCV positive
  • Known Homozygotia (C282Y+/+)
  • Important hepatocytary iron overload for patient with resection
  • HCC non histologically prooved

结局指标

主要结局

Existence of HCC and Pangenomic analysis of DNA polymorphism

Existence of HCC and determination of which genetic polymorphism are predisposing to HCC or preventing for HCC

次要结局

  • cirrhosis severity (compensated or not)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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