Indian Lung Screening Trial (ILST)
Evaluating the Effectiveness of Low-dose CT Based Lung Cancer Screening Among High-risk Individuals and Availability and Impact of Lung Cancer Care Pathways
研究概览
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Abhishek Shankar, MD
- 电话号码:+919968721213
- 邮箱:doc.abhishankar@gmail.com
学习地点
-
-
National Capital Territory of Delhi
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Delhi、National Capital Territory of Delhi、印度、110029
- Dr Bhimrao Ambedkar Institute Rotary Cancer Hospital, AIIMS, New Delhi, India
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接触:
- Abhishek Shankar, MD
- 电话号码:+919968721213
- 邮箱:doc.abhishankar@gmail.com
-
首席研究员:
- Abhishek Shankar, MD
-
-
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Individuals with a history of smoking at least 20 pack-years
- either current smokers or those who quit within the last 15 years
Exclusion Criteria:
- Person who smoked fewer than 100 cigarettes in their lifetime
- individuals currently receiving treatment for active cancer
学习计划
研究是如何设计的?
设计细节
- 主要用途:放映
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
其他:LDCT
Low Dose CT Scan for lung cancer screening
|
Participants will undergo comprehensive baseline lung health assessments including clinical examination and questionnaire administration, followed by an LDCT scan. Participants with positive LDCT findings will be referred immediately to a multidisciplinary team (MDT) for further management. If the baseline LDCT is indeterminate, the participant will undergo a Nodule Follow-Up CT (NFU CT). A positive NFU CT will prompt MDT referral. In cases where the NFU CT remains indeterminate, a second NFU CT will be performed. A positive result at this stage will also result in MDT referral, while a negative result will lead to re-assessment during the next scheduled screening round. |
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 |
|---|---|---|
|
Screen Positive Rate
大体时间:0, 12, 24 months
|
Screen positive rate of LDCT based lung cancer screening in a high-risk Indian population
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0, 12, 24 months
|
|
Screen positive rate for LDCT in the early detection of lung cancer in a high-risk Indian population
大体时间:0, 12, 24 months
|
0, 12, 24 months
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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