Vanderbilt Hereditary Colorectal Cancer Registry
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 730
- 试验地点
- 3
- 主要终点
- Identification of patients at high risk of developing hereditary colorectal cancer
研究概览
简要总结
RATIONALE: Gathering medical and family history information from patients and family members may help doctors better understand hereditary colorectal cancer and hereditary polyposis syndrome and identify patients at high risk of developing hereditary colorectal cancer.
PURPOSE: This research study is collecting information from patients and family members with hereditary colorectal cancer or polyposis syndrome or who are at high risk of developing hereditary colorectal cancer.
详细描述
OBJECTIVES:
Primary
- To identify patients and their family members who have either hereditary colorectal cancer or polyposis syndrome or are at high risk for developing hereditary colorectal cancer.
Secondary
- To establish a tissue and data repository that will be used to further research in hereditary colorectal cancer syndromes.
研究设计
- 研究类型
- Observational
- 观察模型
- Other
- 时间视角
- Prospective
入排标准
- 年龄范围
- — 至 100 Years（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
结局指标
主要结局
Identification of patients at high risk of developing hereditary colorectal cancer
时间窗: continuous data collection
Database will continue indefinitely with IRB approval and investigator support
次要结局
- Establishment of a tissue and data repository(continuous data collection)
研究者
Molly Cone
Assistant Professor
Vanderbilt University Medical Center