跳至主要内容
临床试验/NCT04961125
NCT04961125招募中不适用

Multicenter Study on the Pathogenic Germline Gene Variants of Colorectal Polyposis in China

Second Affiliated Hospital, School of Medicine, Zhejiang University5 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2021年8月2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
200
试验地点
5
主要终点
germline variant detection rate in the polyposis population

研究概览

简要总结

Patients suspected of adenomatous polyposis were included. The criteria used were more than 10 polyps observed under colonoscopy, and pathological confirmation of adenoma. Clinical data and pedigree information were collected. The variants of 139 genes associated with different hereditary cancers and polyposis were screened by NGS, which was performed by Genetron Health on the HiSeqX-ten sequencing platform.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • clinical diagnosis of adenomatous polyposis;
  • enough samples (provide at least 5ml of peripheral whole blood) for germline variant detection

排除标准

  • genetic diagnosis of polyposis syndrome

结局指标

主要结局

germline variant detection rate in the polyposis population

时间窗: through study completion, an average of 3 years

germline variant detection rate in the polyposis population

次要结局

未报告次要终点

研究者

发起方
Second Affiliated Hospital, School of Medicine, Zhejiang University
申办方类型
Other
责任方
Sponsor

研究点 (5)

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