Deep Learning Signature for Predicting Occult Nodal Metastasis of Clinical N0 Lung Cancer

  • STATUS
    Recruiting
  • End date
    Dec 31, 2023
  • participants needed
    5000
  • sponsor
    Shanghai Pulmonary Hospital, Shanghai, China
Updated on 7 October 2022
ct scan
metastasis
lung carcinoma

Summary

The purpose of this study is to compare the predictive performance of a PET/CT-based deep learning signature with the tumor maximum standardized uptake value (SUVmax) on PET for occult nodal metastasis prediction of clinical stage N0 non-small cell lung cancer in a multicenter prospective cohort.

Details
Condition Non-small Cell Lung Cancer
Treatment PET/CT-based Deep Learning Signature
Clinical Study IdentifierNCT05425134
SponsorShanghai Pulmonary Hospital, Shanghai, China
Last Modified on7 October 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

(1) Participants scheduled for surgery for radiological finding of pulmonary lesions from
the preoperative thin-section CT scans; (2) The maximum short-axis diameter of lymph nodes
less than 1 cm on CT scan; (3) The SUVmax of hilar and mediastinal lymph nodes less than
5; (4) Pathological confirmation of primary NSCLC; (5) Age ranging from 20-75 years; (6)
Obtained written informed consent

Exclusion Criteria

(1) Multiple lung lesions; (2) Poor quality of PET-CT images; (3) Participants with
incomplete clinical information; (4) Participants not receiving systematic lymph node
dissection; (5) Participants who have received neoadjuvant therapy before initial PET-CT
evaluation
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Browse trials for

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note