Skip to content

CT Biomarkers Identification by Artificial Intelligence for COVID-19 Prognosis

Identification of Thoracic CT Scan Biomarkers by Deep Learning for Evaluating the Prognosis of Patients With COVID-19 Disease

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04418245
Acronym
COVID 19-IA
Enrollment
0
Registered
2020-06-05
Start date
2020-03-01
Completion date
2021-09-30
Last updated
2025-03-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid-19

Keywords

low dose CT scan, biomarkers, artificial intelligence

Brief summary

The study hypothesis is that low-dose computed tomography (LDCT) coupled with artificial intelligence by deep learning would generate imaging biomarkers linked to the patient's short- and medium-term prognosis. The purpose of this study is to rapidly make available an early decision-making tool (from the first hospital consultation of the patient with symptoms related to SARS-CoV-2) based on the integration of several biomarkers (clinical, biological, imaging by thoracic scanner) allowing both personalized medicine and better anticipation of the patient's evolution in terms of care organization.

Interventions

DIAGNOSTIC_TESTImaging by thoracic scanner

Low-dose computed tomography

Sponsors

Centre Hospitalier Universitaire de Nīmes
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients positive for SARS-CoV-2 according to RT-PCR test between 1st March and 31st May 2020 * Patients undergoing low dose CT scan to establish Covid-19 lung damage * Available for at least 8 days follow-up

Exclusion criteria

• Patients opposing the retrospective use of their data

Design outcomes

Primary

MeasureTime frameDescription
Vital statusDay 8Dead/alive
Patient requiring more than 3 liters of oxygen to maintain a saturation >95% (intensive care unit or resuscitation department)Day 8Yes/no
Percentage of lung affected on CTDay 0% ground glass and condensation calculated by deep learning
Percentage of lung affected by ground glass opacity on scanDay 0% calculated by deep learning
Percentage of lung affected by condensation on scanDay 0% calculated by deep learning

Secondary

MeasureTime frameDescription
Percentage of lung affected on CTDay 16% ground glass and condensation calculated by deep learning
Percentage of lung affected by ground glass opacity on scanDay 16% calculated by deep learning
Percentage of lung affected by condensation on scanDay 16% calculated by deep learning
Software operating timeEnd of study (August 2020)Speed of image loading and image processing depending of brand of scanner
C-reactive protein levelsAdmission Day 0mg/L
lactate dehydrogenaseAdmission Day 0U/L
lymphocytemiaAdmission Day 0g/L
D Dimers levelAdmission Day 0µg/L
Time until onset of symptomsAdmission Day 0Days
Current or previous history of smokingAdmission Day 0Yes/no:
AgeAdmission Day 0Years
BMI> 30Admission Day 0Yes/no:
Medical history of cardiovascular diseaseAdmission Day 0Yes/no: hypertension, coronary artery disease, congestive heart failure, cardiac arrhythmia
DiabetesAdmission Day 0Yes/no
Medical history of respiratory diseaseAdmission Day 0Yes/no: Chronic obstructive pulmonary disease, chronic respiratory failure
Medical history of immunosuppressed conditionAdmission Day 0Yes/no: steroid use, pre-existing immunological condition, current chemotherapy for cancer
Calculate a prognostic score from clinical, biological and CT parametersDay 8Deep learning algorithm
Calculate a prognostic score from clinical and biological parameters onlyDay 8Deep learning algorithm
Compare receiver operating curves of prognostic scores with and without CT parametersDay 8
Time between RT-PCR positive results and first scanAdmission Day 0Hours
Vital statusDay 16Dead/alive
Length of hospitalizationMaximum 30 daysDays
rehospitalizationDay 30Yes/no
Duration of intubationDay 30Days

Countries

France, Martinique

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026