Actively Recruiting

Age: 20Years - 80Years
All Genders
NCT05830812

Improving the Intraoperative Diagnosis Accuracy of Invasiveness for Small-sized Lung Adenocarcinoma

Led by Union Hospital, Tongji Medical College, Huazhong University of Science and Technology · Updated on 2024-09-19

3000

Participants Needed

1

Research Sites

208 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this observational study is to improve the intraoperative diagnosis accuracy of invasiveness for small-sized lung adenocarcinoma by combining multi-modal information. The main question it aims to answer is whether multi-modal information have great value of prediction on the invasiveness for small-sized lung adenocarcinoma. Since a promising limited resection is largely based on intraoperative frozen section diagnosis, there is a growing demand on the high-accuracy of timely pathology diagnosis. The multi-modal information of participants will be collected retrospectively.

CONDITIONS

Official Title

Improving the Intraoperative Diagnosis Accuracy of Invasiveness for Small-sized Lung Adenocarcinoma

Who Can Participate

Age: 20Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • CT examination within 3 months before surgery
  • Patients with operable clinical stage I lung cancer
  • No previous treatment in the lungs or any other organ
  • 20 to 80 years old
  • Tumor less than 3 cm in diameter on thin-slice (0.625-1 mm) CT images
  • Lung adenocarcinoma confirmed by surgical resection and histopathological diagnosis
Not Eligible

You will not qualify if you...

  • Marked artifacts on CT images
  • History of preoperative treatment
  • Incomplete clinical information or DICOM images
  • History of other malignant tumors
  • Lung cancer associated with cystic airspaces

AI-Screening

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Trial Site Locations

Total: 1 location

1

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Wuhan, Hubei, China, 430022

Actively Recruiting

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Research Team

X

Xueyun Tan, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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