- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05221814
Pathological Classification of Pulmonary Nodules in Images Using Deep Learning
January 23, 2022 updated by: Haiyu Zhou, Jiangxi Provincial Cancer Hospital
Pathological Classification of Pulmonary Nodules From Gross Images of Tumor Using Deep Learning
This study aimed to develop a deep-learning model to automatically classify pulmonary nodules based on white-light images and to evaluate the model performance.
Besides, suitable operation could be chosen with the help of this model, which could shorten the time of surgery.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
All white-light photographs of pulmonary nodules from phones of pathologically confirmed adenocarcinoma in situ (AIS), minimally invasive adenocarcinoma (MIA) and invasive adenocarcinoma (IAC) were retrospectively collected from consecutive patients who underwent surgery between June 30, 2020 and September 15, 2021 at Guangdong Provincial People's Hospital.Finally, a total of 1037 white-light images from 973 individuals were included in the study.
The entire dataset was divided into training and test datasets, which were mutually exclusive, using random sampling.
Of these, 830 images were used as the training dataset and 104 images from were used as the test dataset.
The CNN model was used in classifying images, namely, Resnet-50.
For the CNN model, pretrained model with the ImageNet Dataset were adopted using transfer learning.
After constructing the CNN models using the training dataset, the performance of the models was evaluated using the test dataset and the prospective validation dataset.
Study Type
Observational
Enrollment (Anticipated)
2000
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: Haiyu Zhou
- Phone Number: +8613710342002
- Email: lungcancer@163.com
Study Contact Backup
- Name: Shaowei Wu
- Phone Number: +8613411965219
- Email: shaoweiwu0401@gmail.com
Study Locations
-
-
Guangdong
-
Guangzhou, Guangdong, China, 510000
- Recruiting
- Guagndong Provincial People's Hospital
-
Contact:
- Haiyu Zhou, PhD
- Phone Number: *8613710342002
- Email: lungcancer@163.com
-
-
Jiangxi
-
Nanchang, Jiangxi, China, 330000
- Recruiting
- Jiangxi Cancer Hospital
-
-
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 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients in Guangdong Provincial People's hospital from June 30, 2020 to September 15, 2021.
Description
Inclusion Criteria:
- Male or female,18 years and older.
- Patients haven't undergone any therapy.
- The pulmonary nodules were confirmed AIS, MIA or IAC.
- The sizes of pulmonary nodules were less than 3cm.
- The images were jpg format.
Exclusion Criteria:
- Suffering from other tumor disease before or at the same time.
- Images with poor quality or low resolution that precluded proper classification.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
1. Pathological subtype
Time Frame: through study completion, an average of 2 year
|
According to WHO classification of pulmonary tumors in 2020, this study classify pulmonary tumors into adenocarcinoma in situ (AIS), minimally invasive adenocarcinoma (MIA) and invasive adenocarcinoma (IAC).
We would collect the reports of pathological type of pulmonary nodules after surgery.
|
through study completion, an average of 2 year
|
Area Under the Curve (AUC)
Time Frame: through study completion, an average of 2 year
|
The area under the ROC curve based the predicton efficency of model
|
through study completion, an average of 2 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Haiyu Zhou, Guangdong Provincial People's Hospital
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)
June 1, 2020
Primary Completion (Anticipated)
June 1, 2022
Study Completion (Anticipated)
January 1, 2023
Study Registration Dates
First Submitted
January 5, 2022
First Submitted That Met QC Criteria
January 23, 2022
First Posted (Actual)
February 3, 2022
Study Record Updates
Last Update Posted (Actual)
February 3, 2022
Last Update Submitted That Met QC Criteria
January 23, 2022
Last Verified
January 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2021ky228
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Yes
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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.
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