NCT01591512终止不适用
A Prospective Longitudinal Collection of Subjects Diagnosed With Small Cell
适应症
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 4
- 试验地点
- 4
研究概览
简要总结
The purpose of this study is to collect samples to evaluate the ProGRP and NSE assays independently as aids for monitoring the course of disease and therapy in subjects diagnosed with SCLC.
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
- 否
入选标准
- •Confirmed diagnosis of SCLC or mixed SCLC/non-SCLC per histopathology results
- •Scheduled to undergo first-, second- or third-line treatment for SCLC, including chemotherapy, chemotherapy + radiation therapy, or combined concurrent chemoradiotherapy.
- •Able to understand and willing to provide Informed Consent
排除标准
- •No diagnosis of SCLC
- •Not scheduled to undergo treatment for the diagnosis of SCLC
- •Unable to provide Informed Consent
研究者
研究点 (4)
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