AI reads CT scans to predict which lung nodules turn cancerous
NCT ID NCT07647692
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study will develop an artificial intelligence model that uses a patient's series of CT scans over time to predict whether a lung nodule will grow or become cancerous. Researchers will analyze scans from nearly 5,000 people to train the AI to recognize different growth patterns. The goal is to help doctors decide which nodules need treatment and which can be safely monitored. No experimental treatments are given; all scans are part of routine care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this AI model could help doctors better predict which lung nodules are likely to become cancerous, allowing earlier treatment and reducing unnecessary procedures.
- What could go wrong
- This is an observational study, not a treatment trial. The AI model is still being developed and validated, so it may not be accurate enough for widespread use. Results may vary across different patient groups.
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.
- Participants
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About 4,750 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2031
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
Adult patients (≥ 18 years) with a persistent pulmonary ground-glass nodule who underwent routine chest CT surveillance at the participating centers. Three retrospective cohorts (surgical development, surgical internal test, non-surgical internal test) are identified from the institutional PACS and clinical records of Peking University People's Hospital; one prospective multi-center cohort is enrolled consecutively after the AI model is locked.
- 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.
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: * Age ≥ 18 years. * Persistent pulmonary ground-glass nodule (pGGN or mGGN, 5-30 mm) on thin-slice chest CT (slice thickness ≤ 1.5 mm). * Baseline and follow-up thin-slice chest CTs of sufficient quality for 3D segmentation and registration. * Minimum interval between any two consecutive CTs \> 1 month. * Complete baseline clinical data available (age, sex, smoking history, family history of malignancy, relevant comorbidities). Cohort-specific inclusion * Group 1 (Development): surgical resection of the target GGN at PKUPH between Jan 2007 - Jun 2025, with ≥ 2 pre-operative thin-slice CTs available. * Group 2 (Surgical internal test): surgical resection at PKUPH between Jul 2025 - Jan 2026, with ≥ 2 pre-operative thin-slice CTs available. * Group 3 (Non-surgical internal test): non-operative management at PKUPH between Jan 2020 - Dec 2025, with ≥ 3 thin-slice CTs of the target GGN available. * Group 4 (Prospective external validation): prospective enrollment after model lock at participating centers, baseline CT plus ≥ 2 planned routine follow-up thin-slice CTs. Exclusion Criteria: * Coexisting severe pulmonary disease that obscures evaluation of the target GGN (e.g., active pulmonary tuberculosis, severe interstitial lung disease). * Prior history of any other thoracic malignancy, or active extrathoracic malignancy under treatment within 5 years, that would confound interpretation of the target GGN. * CT image quality insufficient for registration and feature extraction (severe motion artifact, slice thickness \> 1.5 mm at any required timepoint, or extensive metallic artifact projecting over the target GGN). * Pure solid nodule with no ground-glass component. * Target GGN already received treatment (resection, ablation, or radiotherapy) prior to the baseline CT used in this study.
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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 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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Peking University People's Hospital
Beijing, Beijing Municipality, 100044, China
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