- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05471869
Computational Imaging Research Based on Deep Learning
July 21, 2022 updated by: Xin Lou, Chinese PLA General Hospital
Computational Imaging Using Pixel-level Graph Adversarial Learning
Computational imaging research based on deep learning
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
Based on the current technical challenges, subject development and upgrade of knowledge, to avoid the occurrence of adverse medical accidents, simplify the diagnostic process, artificial intelligence has become the alternative method of choice, by constructing training deep learning model, the CTA as model inputs aneurysm detection and diagnosis to improve diagnosis effectiveness, promote the development of medical technology
Study Type
Observational
Enrollment (Anticipated)
1200
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
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Beijing, China, 100853
- Chinese PLA General Hospital
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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
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
varity of people
Description
Inclusion Criteria:
- Age: 18-80 years.
- CT paired imaging data of vessels, including layer-to-layer plain CT and enhanced CT. 2 Time range: January 2010 to December 2021.
- Scanning sites: CT and CTA of head, neck, chest, abdomen or iliac.
Exclusion Criteria:
- Unpaired CT image .
- Severe artifact CT image.
- enhancement CT failure image (failure to capture arterial phase or poor arterial development, insufficient flow of contrast agent, etc.)
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 |
|---|---|---|
|
Objective evaluation
Time Frame: 30 minutes
|
using SSIM\MAE index evaluation
|
30 minutes
|
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)
November 1, 2021
Primary Completion (ANTICIPATED)
July 30, 2022
Study Completion (ANTICIPATED)
August 15, 2022
Study Registration Dates
First Submitted
July 21, 2022
First Submitted That Met QC Criteria
July 21, 2022
First Posted (ACTUAL)
July 25, 2022
Study Record Updates
Last Update Posted (ACTUAL)
July 25, 2022
Last Update Submitted That Met QC Criteria
July 21, 2022
Last Verified
July 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Synthesis imaging-ChinaPLAGH
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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.