Laser and AI join forces to spot aggressive lung cancer
NCT ID NCT07799038
First seen Sep 02, 2026 · Last updated Sep 03, 2026 · Updated 1 time
Summary
This trial tests whether a new imaging method, using femtosecond laser light and artificial intelligence, can accurately predict high-risk features in lung cancer, such as spread to lymph nodes. Researchers will compare the AI's predictions with actual pathology results from surgical specimens. The study involves 333 adults with lung nodules who are scheduled for surgery. If the method works, it could help doctors make more informed treatment decisions without waiting for traditional lab tests.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Femtosecond laser label-free imaging combined with artificial intelligence
- What this could lead to
- If successful, this could provide a faster, more accurate way to predict whether lung cancer has spread to lymph nodes, helping doctors tailor surgery and treatment.
- What could go wrong
- This is an early diagnostic study, and the technology may not prove accurate enough for routine use. Results are blinded and won't affect patient care during the trial.
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 333 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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Aug 2028
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
Lung cancer patients undergoing pulmonary resection.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
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: 1. Pulmonary nodules detected by clinical imaging with an indication for surgical resection. 2. Patient agrees to and is planned for pulmonary (partial) resection. 3. Resected specimens are suitable for FLI imaging. 4. Written informed consent obtained from the patient or legal representative. 5. Patients undergoing pulmonary (partial) resection at our hospital during this study. Exclusion Criteria: 1. Insufficient sample. 2. Specimen with crushing, contamination, or improper preservation, precluding valid imaging as judged by the investigator. 3. Inability to obtain matched pathology results corresponding to FLI images. 4. Inability to obtain final pathological diagnosis. 5. Other conditions deemed by the investigator as unsuitable for study participation.
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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
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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.
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Other studies related to the condition(s) this trial covers.
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