AI learns to read scans and reports for smarter disease diagnosis
NCT ID NCT07445152
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aims to create an artificial intelligence (AI) system that can combine medical images (like CT and MRI scans) with patient records and lab results to help doctors more accurately diagnose diseases of the liver, gallbladder, and pancreas. The researchers will use data from 2,000 adult patients to train and test the AI. The goal is to make diagnosis faster and more reliable, not to provide a new treatment.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 2,000 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Nov 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
he study population was composed of adult patients who met the preset inclusion criteria and were free of any exclusion criteria. In terms of inclusion requirements, eligible patients were aged 18 years or older and had received imaging examinations including computed tomography (CT), magnetic resonance imaging (MRI), or ultrasound at the hospital during the study period. The examination items were required to target the hepatobiliary and pancreatic system, which was the focus of the research. All enrolled patients needed to be equipped with at least complete imaging data and radiological diagnostic reports, with relevant medical record information serving as supplementary modalities. In addition, written informed consent must be obtained from the patients themselves or their legal representatives, who agreed that the de-identified data of the patients could be used for the validation of scientific research models. Finally, all case data of the selected patients had to pass strict qual
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult patients aged ≥ 18 years. * Patients who underwent imaging examinations (CT, MRI, ultrasound, etc.) at this hospital during the study period. * The examination items are consistent with the disease types or systems focused on by the study (hepatobiliary and pancreatic system). * Possess at least complete imaging data, radiological diagnostic reports, with relevant medical record information as supplementary modalities. * Patients and their legal representatives have signed an informed consent form, agreeing to the use of their de-identified data for scientific research model validation. Exclusion Criteria: * Patients who refuse to sign the informed consent form. * Cases with unassessable images due to severe motion artifacts, incomplete scanning, or equipment abnormalities. * Cases with severe deficiency of clinical data or failure to match with imaging data. * Cases with special pathological conditions or post-operative status (e.g., extensive resection, significant structural changes after radiotherapy) that affect the consistency of model analysis. * Data samples with privacy protection or legal risks.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
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