KCT0007987尚未招募未知
Multicenter clinical evaluation study of clinical effectivity of AptoDetectTM-Lung for Auxiliary diagnostics of Non-Small Cell Lung Cancer [Apto_RADS]
Kyung Hee University Hospital0 个研究点目标入组 2,994 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 2,994
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 19(Year) 至 o Limit(—)
- 性别
- All
入选标准
- •1) A patient who has given written consent to participate in this study
- •2) Adult men and women over 19 years of age
- •3) Patients with solid nodules or part solid nodules corresponding to categories 3 to 4 according to the Lung-RADS® version 1.1 pulmonary nodule categorization guidelines
- •However, patients in category S according to the Lung-RADS® version 1.1 pulmonary nodule categorization guidelines can also be enrolled.
排除标准
- •1) Patients with ground glass nodules (GGO) in the Lung-RADS® version 1.1 pulmonary nodule categorization guidelines
- •2) Any pulmonary infection requiring current treatment (both oral or intravenous)
- •However, if the researcher determines that treatment for lung infection has been completed, enrollment is possible.
- •3) Patients with histologically confirmed malignant tumors prior to participation in this study
- •However, registration is possible in the following cases, but registration is not possible if the patient is accompanied by a malignant tumor requiring current treatment.
- •? Cases confirmed as malignant tumors (including lung cancer) but in remission for more than 5 years after completion of treatment
- •? Effectively treated non-melanoma skin cancer, cervical carcinoma in situ, mammary ductal carcinoma in situ, localized prostate cancer treated for curative purposes, and thyroid cancer can be registered.
- •4) Pregnant women
研究者
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