A Multi-Centered Trial Evaluating the Role of Vitamin D Metabolism in Non-Small Cell Lung Cancer (EBUS)
研究概览
地位
条件
详细说明
This study seeks to prospectively determine the relationship between Vitamin D gene expression and median survival as a primary outcome, and the relationships between the Vitamin D receptor (VDR)/CYP24A1 gene expression and cancer stage, smoking status, serum 1,25 (OH)2D3 levels as well as CYP24A1 genotype.
Patients who are suspected to have lung cancer will be recruited to this study prior to their diagnostic biopsy. Those who have consented to the study will give permission for blood and tissue from this biopsy to be analyzed for the study endpoints. Statistical analysis on this data will seek to correlate CYP24A1 expression and medican survival of the participants. Patients' data will be collected for smoking status and cancer stage.
Study enrollment to adequately power the study statistically is 80 patients. Anticipated study duration is from 12 months to 18 months for sample collection and two years for follow-up for patient survival.
研究类型
注册 (实际的)
联系人和位置
学习地点
-
-
Michigan
-
Ann Arbor、Michigan、美国、48109
- University of Michigan Cancer Center
-
Ann Arbor、Michigan、美国、48105
- United States Department of Veteran's Affairs Medical Center
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
描述
Inclusion Criteria:
- Scheduled for diagnostic bronchoscopy for suspected advanced stage lung cancer by CT/PET scanning.
- Tumor or lymph node accessible by transbronchial needle aspiration.
- Age 18-80.
- All patients must be informed of the investigational nature of this study and must give written informed consent in accordance with institutional and federal guidelines.
Exclusion Criteria:
- Unstable cardiovascular disease or other systemic disease
- Mental incompetence/active psychiatric illness
- Medical contraindication for bronchoscopy
学习计划
研究是如何设计的？
设计细节
队列和干预
团体/队列 |
|---|
|
Observational Group
NSCLC subject undergoing bronchoscopy
|
研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Time to lung cancer related death
大体时间：18 months
|
Time to lung cancer related death
|
18 months
|
合作者和调查者
调查人员
- 首席研究员：Nithya Ramnath, MD、University of Michigan Medical Center and Veteran's Administration Health Center
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.