跳至主要内容
临床试验/NCT00516230
NCT00516230Unknown不适用

Establishing Effective Screening Methods for Diagnosing Hereditary Nonpolypoisis Colorectal Cancer

Samsung Medical Center1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2006年1月最近更新:
适应症

试验速览

阶段
不适用
入组人数
200
试验地点
1

研究概览

简要总结

Correct identification of Lynch syndrome at the time of colorectal cancer presentation is important. We aim to find best ways to screen patients with colorectal cancer in Korea.

详细描述

Patients with newly diagnoised colorectal cancer will be eligible. They will undergo detailed history taking including family history, and molecular stuidies including microsatellite instability test and immunohistochemistry for DNA mismatch repair protein with pre-selection. Any abnormal finding in molecular stuides will be offered genetic testing (after testing methylation status for patients with abnormalities in MLH1).

研究设计

研究类型
Observational
观察模型
Defined Population
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Colorectal cancer

排除标准

  • Histology showing other than adenocarcinoma

研究者

申办方类型
Other

研究点 (1)

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