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临床试验/KCT0007987
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

发起方
Kyung Hee University Hospital

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