New screening method aims to catch lung cancer earlier in asbestos workers
NCT ID NCT01687647
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether analyzing sputum (phlegm) with automated cytometry, combined with low-dose CT scans and blood tests, could better detect lung cancer in workers heavily exposed to asbestos. The goal was to reduce false positives and improve early diagnosis. The trial involved 463 participants but was terminated early, so its full potential remains unclear.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- low-dose CT-scan, induced sputum sample, and blood test
- What this could lead to
- If successful, this approach could improve early lung cancer detection in high-risk asbestos workers while reducing unnecessary follow-ups from false alarms.
- What could go wrong
- The study was terminated early, so results are limited. The methods are still experimental and may not be better than current screening practices.
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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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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463 people
The number who actually took part.
- Start date
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Sep 2012
- Finished
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Oct 2020
- 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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56 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: * High professional asbestos exposure * Member of a former cohort recruited between 2000 and 2006 in Caen, Rouen and Le Havre (inclusion criteria: 50-75 years at the time of initial recruitment, high intermittent asbestos exposure \>= 1 year, or high discontinuous asbestos exposure \>=10 years). All the living members of the cohort will be contacted: a maximum of 1000 subjects is expected, probably less. * Informed consent signed Exclusion Criteria: * Personal history of lung cancer * Refusal of the study protocol * Uncontrolled asthma or lung failure
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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.
Contacts and locations
Locations
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Caen University Hospital
Caen, 14000, France
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Le Havre Hospital
Le Havre, 76600, France
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Rouen University Hospital
Rouen, 76031, France
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