- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04000620
Imaging-based Deep Learning for Lung Cancer Diagnosis and Staging
November 15, 2021 updated by: Yang Jin, Wuhan Union Hospital, China
The Role of CNN Architecture-based Transfer Learning of Medical Imaging in Lung Cancer Diagnosis and Staging
Lung cancer diagnosis and staging are two fundamental and critical issue in clinical lung cancer management and therapeutic decision-making.
Invasive procedures for pathologic analysis are gold standard for diagnosis and staging, however, invasive procedures related-complications are inevitable.
Noninvasive medical imaging is a powerful tool, however there is almost no room for improvement just according to the experience of radiologist and clinician.
The researchers will investigate the role of computer based deep learning of medical imaging in the diagnosis of lesion of lung, lymph node and other sites suspected with metastasis.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Radiologist
Study Type
Observational
Enrollment (Anticipated)
500
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Zhilei Lv, MD
- Phone Number: 86-15107177084
- Email: 794646434@qq.com
Study Locations
-
-
Hubei
-
Wuhan, Hubei, China, 430000
- Recruiting
- Wuhan Union Hospital
-
Contact:
- Zhilei Lv, MD
- Phone Number: 86-15107177084
- Email: 794646434@qq.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Lung cancer patients with PET/CT or CT examination before any cancer-specific treatment
Description
Inclusion Criteria:
- Pathological diagnosis of lung cancer
- PET/CT or CT examination before any cancer-specific treatment
Exclusion Criteria:
- A history of other malignancies
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
cancer cell involvement predicted by deep learning
the participants with lesions of lung, lymph node or other sites predicted as positive for cancer cell involvement by imaging based deep learning.
|
treatment intent surgery
diagnostic punture
|
|
no cancer cell involvement predicted by deep learning
the participants with lesions of lung, lymph node or other sites predicted as negative for cancer cell involvement by imaging based deep learning.
|
treatment intent surgery
diagnostic punture
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
pathologic result revealed cancer cell involvement in lesion
Time Frame: 1 month after the pathologic test
|
1 month after the pathologic test
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 1, 2018
Primary Completion (Anticipated)
December 30, 2021
Study Completion (Anticipated)
May 1, 2024
Study Registration Dates
First Submitted
June 24, 2019
First Submitted That Met QC Criteria
June 24, 2019
First Posted (Actual)
June 27, 2019
Study Record Updates
Last Update Posted (Actual)
November 16, 2021
Last Update Submitted That Met QC Criteria
November 15, 2021
Last Verified
November 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AFDSFA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.