NCT01098552已完成不适用
Participation in Procurement of Tissue, Serum, Plasma, Cell Bank, DNA and RNA Samples, and Urine for Biological Studies Related to Prostate Cancer and Prostate Cancer Treatment Follow Up
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Mayo Clinic
- 入组人数
- 4,900
- 试验地点
- 1
研究概览
简要总结
This research study is being done to collect regular and routine follow-up information related to the outcome of treatment for prostate cancer.
This study is also being done to relate treatment outcome to measurement of substances in the blood such as prostate-specific antigen (PSA) and other markers. Also environmental and genetic factors that might be responsible for prostate cancer are being investigated.
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
- Male
- 接受健康志愿者
- 否
入选标准
- •Informed consent explained and signed prior to any study related procedures.
- •Age ≥18 years
- •Eastern Cooperative Oncology Group (ECOG) performance status of 2 or better, or Karnofsky performance of 60% or better.
- •Histologically confirmed adenocarcinoma of the prostate within 10 years of study entry.
- •Willingness to return to Mayo Clinic Rochester for follow-up or participate in mail-in PSA processing.
- •Must be disease-free from a previous diagnosis of cancer for a period of time = 5 years excluding cutaneous malignancies of squamous cell or basal cell carcinoma.
排除标准
- •Life expectancy < 5 years.
- •Inability to return to Mayo Rochester for follow-up appointments, sera, and urine collection per protocol.
- •Previous or a concurrent diagnosis of cancers other than basal cell or invasive squamous cell carcinoma of skin within the past 5 years.
研究者
研究点 (1)
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