Feasibility and Effectiveness of Respiratory Movement Management in Lung Cancer Receiving Stereotactic Radiotherapy Using a Novel Positional Fixation Device (E20241186)
A Single Center, Translational Study on the Feasibility and Effectiveness of Respiratory Movement Management in Lung Cancer Patients Receiving Stereotactic Radiotherapy Using a Novel Positional Fixation Device
The purpose of this clinical trial is to understand the safety and effectiveness of abdominal pressure devices in inhibiting respiratory movement in lung cancer patients. The main question it aims to answer is:
Did the abdominal pressure device reduce the respiratory movement of participants with lung cancer tumors?
Participants will:
Record how much they use abdominal pressure devices to suppress lung cancer tumor respiratory movement
研究概览
研究类型
注册 (估计的)
联系人和位置
学习联系方式
- 姓名：Xuyao Yu Dr
- 电话号码：86-022-23341405
- 邮箱：yuxuyao@tmu.edu.cn
学习地点
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Tianjin、中国
- 招聘中
- Tianjin Medical University Cancer Institute and Hospital
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接触：
- Xu Yao Yu
- 电话号码：+862223340123
- 邮箱：yuxuyao@tmu.edu.cn
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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
取样方法
研究人群
描述
Inclusion Criteria:
Clinical diagnosis is solitary peripheral lung cancer, and after comprehensive evaluation by the participating physicians based on the patient's clinical data, it is suitable for receiving SBRT treatment;
Exclusion Criteria:
Central or super central lung cancer patients who are intolerant or unwilling to undergo respiratory suppression and chest and abdominal compression fixation
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 |
干预/治疗 |
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Breathing management group
CT/4DCT scan under breathing management
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Abdominal compression suppresses respiratory movement in patients
Apply pressure to the patient's abdomen to achieve respiratory movement inhibition
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No breathing management group
CT/4DCT scan under free breathing
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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 |
|---|---|---|
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Tumor displacement range
大体时间：Within 6 months after enrollment
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Based on 4DCT for delineating tumor motion range and extracting radiomics features in patients with and without respiratory management
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Within 6 months after enrollment
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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
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.
肺癌，非小细胞的临床试验
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Taichung Veterans General Hospital完全的心脏毒性 | 非小细胞肺癌（MeSH术语：Carcinoma, Non-Small-Cell Lung） | 药物相关副作用和不良反应（MeSH术语） | 表皮生长因子受体酪氨酸激酶抑制剂台湾
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Fondazione del Piemonte per l'Oncologia招聘中乳腺癌 | 卵巢癌 | 结直肠癌 | 黑色素瘤（皮肤癌） | 非小细胞肺癌（MeSH术语：Carcinoma, Non-Small-Cell Lung）意大利