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临床试验/NCT01667952
NCT01667952已完成不适用

Prospective Ascertainment for Late Effects Among Survivors of Cancer, Tumor, or a Related Illness

Memorial Sloan Kettering Cancer Center1 个研究点 分布在 1 个国家目标入组 1,068 人开始时间: 2012年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,068
试验地点
1
主要终点
establish a registry of DNA

研究概览

简要总结

The purpose of this study is to establish a registry of survivors of cancer, tumor, or a related illness.

研究设计

研究类型
Observational
观察模型
Family Based
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • English speaking
  • A personal history of cancer tumor, or a related illness
  • Followed in the the Adult Long Term Follow Up Program, Pediatric Long Term Follow Up Program, or Lymphoma Service at MSKCC

排除标准

  • Evidence of active progression of disease or recurrence
  • Neurocognitive deficits that impair ability to give informed consent.

结局指标

主要结局

establish a registry of DNA

时间窗: 4 years

For the purpose of facilitating future genetic laboratory investigations of late effects among of survivors of cancer, tumors, or a related illness. Patients in the ALTFU Program are followed for secondary malignant neoplasms and other adverse outcomes (so-called "late effects") including cardiomyopathy, pulmonary fibrosis, cardiac valvular pathology, osteoporosis, and others. The following data will be ascertained from each study participant: (1) family history information will be ascertained using the Family History Questionnaire (Appendix A); and (2) saliva or blood samples for genetic analysis.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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