AI trained to spot fake medical images put to the test
NCT ID NCT07823023
First seen Sep 16, 2026 · Last updated Sep 17, 2026 · Updated 1 time
Summary
Researchers are testing whether an AI system called DeepMedFake helps doctors and healthcare auditors decide which medical images need a closer look. The system flags images that may be synthetic or that do not match the patient's information. In this trial, 64 physicians and audit professionals review sets of medical cases with and without the AI's help. The goal is to see whether the AI improves their ability to correctly identify images that require further verification.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- DeepMedFake, an artificial intelligence system that checks medical images for authenticity and patient-image consistency
- What this could lead to
- If it works, this could give hospitals and auditors a faster way to flag suspicious or mismatched medical images before they are used in care or audits.
- What could go wrong
- The trial is small and tests the AI in a controlled reading task, so results may not reflect real-world performance. The system could miss fake images or raise false alarms, and it only assists human reviewers rather than making final calls.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 64 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2026
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.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Aged 18 years or older. * Able to complete reading periods and all required electronic study procedures. * Completed the standardized study training and practice cases. * Provided written informed consent before participation. (1)Hospital clinical cohort participants must also meet the following criteria: * Hold a valid physician qualification. * Currently practice in ophthalmology, radiology, ultrasound medicine, or a clinical specialty in which imaging of the neurological or cerebrovascular, cardiovascular, thoracic, abdominal, or musculoskeletal domain is routinely reviewed. * Have direct professional experience reviewing all imaging modalities and clinical imaging domains assigned to them in the study. * Routinely use the assigned medical images for image interpretation, image verification or clinical decision-making. (2)Healthcare audit cohort participants must also meet the following criteria: * Currently work in healthcare audit, medical reimbursement review, medical-cost review or medical-material verification. * Have experience reviewing medical imaging materials as part of their routine work. * Have knowledge required to interpret the medical images and patient information presented in the study and to determine whether further verification is required. Exclusion Criteria: * Direct involvement in development of the locked DeepMedFake model, determination of model weights or selection of decision thresholds. * Direct involvement in selection or construction of the formal case library or adjudication of the reference standard. * Direct involvement in generation or implementation of the reader randomization sequence. * Previous participation as a reader in the pilot study. * Previous access to any formal study case, case-construction record or reference-standard label. * Access to undisclosed study information that could permit advance identification of case type or image-generation method. * A financial, professional or other conflict of interest considered likely to compromise independent case assessment.
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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 places running it
1 site. The list below names each one and where it is.
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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
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Beijing Friendship Hospital, Capital Medical University
Beijing, Beijing Municipality, 100050, China