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Establishment and application of a risk assessment system for differentiating benign and malignant pulmonary nodules based on AI intelligent imaging and probe labeling technology

Establishment and application of a risk assessment system for differentiating benign and malignant pulmonary nodules based on AI intelligent imaging and probe labeling technology

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000036622
Enrollment
Unknown
Registered
2020-08-24
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-09-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

lung cancer

Interventions

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Sponsors

Ruijin Hospital North, 999 Xiwang Road, Jiading District, Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: The subjects should meet the following criteria: 1. Commitment to follow the research procedures and cooperate with the implementation of the whole process research. 2. Specified gender or age range. 3. According to the diagnosis, symptoms and signs of lung cancer or benign lung disease, or in general good health, can adhere to and cooperate with research intervention, such as chemotherapy. 4. Signed and dated informed consent.

Exclusion criteria

Exclusion criteria: Subjects who met any of the following criteria were excluded from this study: 1. Specific drugs that are not allowed are currently being used. 2. Equipped with a specific device (e.g. cardiac pacemaker). 3. In pregnancy or lactation. 4. New coronavirus infection or other febrile diseases occurred during the follow-up period. 5. Treatment with other trial drugs at a specific time. 6. There are specified diseases or conditions excluded from the study (physical or psychological, physical examination findings). 7. There were serious heart, lung, liver and kidney dysfunction and mental disorders. 8. In the past, we have received clinical therapeutic interventions related to lung cancer, such as surgery, radiotherapy, chemotherapy, targeted therapy, immunotherapy, etc. 9. Because of the sampling problem, it can not meet the requirements of the Research Institute for histopathological examination 10. There was a history of malignant tumor in recent 5 years.

Design outcomes

Primary

MeasureTime frame
CTC;CTC;Canceration;SEN, SPE, ACC, AUC of ROC;

Countries

China

Contacts

Public ContactGu Zhidong

Ruijin Hospital North, Shanghai Jiaotong University, School of Medicine

13801653534@163.com+86 13801653534

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026