跳至主要内容
临床试验/NCT05734430
NCT05734430招募中不适用

Genetics of Appendix Cancer: The GAP Study

Andreana Holowatyj, PhD, MSCI1 个研究点 分布在 1 个国家目标入组 700 人开始时间: 2022年11月11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
700
试验地点
1
主要终点
Prevalence and spectrum of pathogenic and likely pathogenic germline variants in appendix cancer patients and their biological parents

研究概览

简要总结

The GAP Study is a prospective cohort study designed to comprehensively investigate genetic variations that may contribute to cancer development among individuals diagnosed with appendix/appendiceal cancer who are ages 18+ years.

详细描述

The Genetics of Appendix Cancer (GAP) Study aims to analyze hereditary factors, tumor characteristics and clinical features/outcomes among adults diagnosed with appendix cancer and their biological parents. Patients are recruited at any time after a diagnosis of appendix cancer and followed for up to 6 years after study enrollment. This cohort is enriched by robust biospecimens and data collections.

研究设计

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

入排标准

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

入选标准

  • Known diagnosis of appendix cancer in the United States
  • Mentally and physically able to consent and participate in the study
  • GAP Vanderbilt
  • Known diagnosis of appendix cancer
  • Diagnosed by and/or consulting with a physician/clinical provider participating in the GAP Study
  • Mentally and physically able to consent and participate in the study
  • Biological parents (mother and/or father) of individuals actively participating in the GAP Study
  • Residing in the United States
  • Mentally and physically able to consent and participate in the study

排除标准

  • Women pregnant at the time of consent
  • Prisoners
  • Unable to provide informed consent
  • Unable to read, write, or complete questionnaires in English

结局指标

主要结局

Prevalence and spectrum of pathogenic and likely pathogenic germline variants in appendix cancer patients and their biological parents

时间窗: Within 6 years of study enrollment

次要结局

  • Association of germline genetic variants with clinical, pathologic and molecular features of appendix tumors(Within 6 years of study enrollment)

研究者

发起方
Andreana Holowatyj, PhD, MSCI
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Andreana Holowatyj, PhD, MSCI

Sponsor Investigator

Vanderbilt-Ingram Cancer Center

研究点 (1)

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