- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04347369
A Retrospective Study of Neural Network Model to Dynamically Quantificate the Severity in COVID-19 Disease
February 22, 2024 updated by: Jianguo Sun, Xinqiao Hospital of Chongqing
a Retrospective Study of Neural Network Model to Dynamically Quantificate the Severity in COVID-19 Disease
The research aim to collect large samples of COVID-19 disease patients with clinical symptoms, laboratory and imaging examination data.
Screening the biological indicators which are related to the occurrence of severe diseases.
Then, investigators using artificial intelligence (AI) technology deep learning method to find a prediction model that can dynamically quantify COVID-19 disease severity.
Study Overview
Study Type
Observational
Enrollment (Actual)
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
-
-
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Chongqing, China, 400000
- Xinqiao Hospital of Chongqing
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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
N/A
Sampling Method
Probability Sample
Study Population
Patients of COVID-19 disease
Description
Inclusion Criteria:
- Patients of COVID-19 disease confirmed by virus nucleic acid RT-PCR and CT
Exclusion Criteria:
- unconfirmed suspected cases
- Patients during pregnancy and lactation
- incomplete clinical data
- inestigators considered patients ineligible for the trial
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 |
Intervention / Treatment |
---|---|
Observed group
The patients who were detected COVID-19 disease by RT-PCR and CT imaging.
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clinical diagnosis
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
discrimination
Time Frame: up to 3 months
|
The performance of our prediction model is evaluated with the receiver operating characteristic (ROC) curves, areas under the curves (AUCs) and concordance index (c-index).
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up to 3 months
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Calibration
Time Frame: up to 3 months
|
The calibration curves analysis is used to show error between the predicted clinical phenotype with prediction model and actual clinical phenotype.
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up to 3 months
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Net benefit
Time Frame: up to 3 months
|
Decision curve analysis was used to determine whether the models could be considered useful tools for clinical decisionmaking by comparing the net benefits at any threshold.
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up to 3 months
|
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 17, 2020
Primary Completion (Actual)
August 30, 2020
Study Completion (Actual)
December 31, 2020
Study Registration Dates
First Submitted
March 18, 2020
First Submitted That Met QC Criteria
April 12, 2020
First Posted (Actual)
April 15, 2020
Study Record Updates
Last Update Posted (Actual)
February 23, 2024
Last Update Submitted That Met QC Criteria
February 22, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- XQonc-015
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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