- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03954847
Clinical Significance of Computer Aided Image Analysis in Treatment Response Evaluation of Lung Cancer
May 16, 2019 updated by: Yang Jin, Wuhan Union Hospital, China
The investigators will evaluate the utility of computer aided image analysis in lung cancer with the aim of predicting treatment response and prognosis.
Study Overview
Status
Unknown
Conditions
Detailed Description
Tumor biological behavior is the fundamental cause of heterogeneous prognosis.
The features found on medical images are also reflections of the tumor biological behavior.
However, the limitations in spatial and intensity resolution of the naked eye are two inevitable shortcomings of image interpretation by naked eyes, resulting in subjective and limited analyses of images.
Computer aided image analyses such as radiomic analysis and machine learning methods are emerging as promising image interpretation methods.
The natural advantage of the unlimited spatial and intensity resolution of computers can overcome the shortcomings of visual inspection with the naked eye.
Moreover, the massive computing power of computer is also far greater than that of humans.
This study will focus on the application of computer aided analysis in predicting treatment response and prognosis in lung cancer.
Study Type
Observational
Enrollment (Anticipated)
1000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Hubei
-
Wuhan, Hubei, China, 430000
- Recruiting
- Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
-
-
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 and older (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:
- Patients >= 18 years old
- Pathological diagnosis of NSCLC between 2012 and 2019;
- PET/CT or CT examination before any cancer-specific treatment;
Exclusion Criteria:
- A time interval between treatment and image examination greater than 1 month;
- 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
Cohorts and Interventions
Group / Cohort |
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Lung cancer patients
Lung cancer patients with PET/CT or CT examination before any cancer-specific treatment
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Overall survival
Time Frame: 2012-2021
|
The interval between the date of diagnosis and death
|
2012-2021
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Progression free survival
Time Frame: 2012-2021
|
The interval between the date of treatment initiation and disease progression
|
2012-2021
|
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)
January 1, 2012
Primary Completion (Anticipated)
December 31, 2020
Study Completion (Anticipated)
December 31, 2020
Study Registration Dates
First Submitted
May 16, 2019
First Submitted That Met QC Criteria
May 16, 2019
First Posted (Actual)
May 17, 2019
Study Record Updates
Last Update Posted (Actual)
May 17, 2019
Last Update Submitted That Met QC Criteria
May 16, 2019
Last Verified
May 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- WuhanUH-V1.2
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.
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