CT Biomarkers Identification by Artificial Intelligence for COVID-19 Prognosis
NCT ID: NCT04418245
Last Updated: 2025-03-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
WITHDRAWN
OBSERVATIONAL
2020-03-01
2021-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Lung CT Scan Analysis of SARS-CoV2 Induced Lung Injury
NCT04395482
Effectiveness of Ultra-low-dose Chest CT With AI Based Denoising Solution
NCT05398887
A Study to Assess the Impact of an Artificial Intelligence (AI) System on Chest X-ray Reporting
NCT05489471
Evaluation of a COVID-19 Pneumonia CXR AI Detection Algorithm
NCT04561024
Performance of CT Parameters Compared to Bone Mineral Density to Detect Bone Fragility in Rheumatoid Arthritis
NCT04413448
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Patients positive for SARS-CoV-2
Imaging by thoracic scanner
Low-dose computed tomography
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Imaging by thoracic scanner
Low-dose computed tomography
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patients undergoing low dose CT scan to establish Covid-19 lung damage
* Available for at least 8 days follow-up
Exclusion Criteria
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Centre Hospitalier Universitaire de Nīmes
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Julien Frandon
Role: PRINCIPAL_INVESTIGATOR
CHU Nimes
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
CHU la Timone
Marseille, , France
CHU Montpellier
Montpellier, , France
CHU de Nimes
Nîmes, , France
CHU Poitiers
Poitiers, , France
CHU Strasbourg
Strasbourg, , France
CHU Martinique
Fort-de-France, , Martinique
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
NIMAO/2020/COVID 19-IA/JF-01
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.