NCT07042867Not yet recruiting
Prospective Multicenter Cohort Study for the Development and Evaluation of Risk Stratification Tools for Lung Cancers and Their Postoperative Recurrences Using Multimodal Clinical, Radiological, Tissue and Longitudinal Biological Phenotyping Among People at Risk of Lung Cancer
Source: ClinicalTrials.gov · Last updated 29 Jun 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
Interventional study with minimal risks and constraints, involving annual assessment of the prevalence and incidence of lung cancer using low-dose contrast-free thoracic CT scans, immunological, inflammatory, metabolic, blood nucleic acid and digestive microbiota profiles; systematic proposal of smoking cessation for active smokers, or assistance in maintaining cessation This is a prospective validation study of risk stratification tools still under development. The results of this study will be used to design medical devices (software integrating risk stratification tools), which will then be evaluated as part of subsequent Clinical Investigations.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 900 (estimated)
- First submitted
- 20 Jun 2025
- Start date
- 15 Jul 2025
- Primary completion date
- 15 Jan 2028
- Lead sponsor
- Assistance Publique Hopitaux De Marseille
- Diseases
- Lung cancer
- NCT number
- NCT07042867
What you commit to
- Study type: Interventional
- Planned participants: 900
- From 15 Jul 2025 to the primary completion date, 15 Jan 2028
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Goups A and B Contraindication to lung biopsy or thoracic surgery for diagnostic or therapeutic purposes
Other illness
- Group C Eligible for lung cancer screening according to INCa\* criteria
- Symptoms of lung cancer (involuntary weight loss \> 10% of usual weight in 1 year, hemoptysis)
- Known history of pulmonary nodule requiring specialized follow-up
- History of pulmonary fibrosis or pulmonary hypertension
- Active pulmonary parenchymal infection
- Severe cardiac or respiratory insufficiency (rest dyspnea)
Age
- Previous cancer \< 5 years (except carcinoma in situ of the uterine cervix, basal cell carcinoma of the skin, non-invasive urothelial carcinoma treated for curative purposes without CT lung surveillance, prostate cancer with undiagnosable PSA)
Other
- Performance status (WHO) 2, 3 or 4
- All Groups
- patient privé de liberté
- patient sous tutelle ou curatelle
- femmes enceintes ou allaitantes
- patient dans l'incapacité d'effectuer le suivi de 30 mois
Who the study is looking for
- Group A:
- CI 1- Age \> 18 years AND CI2a- Person eligible for screening with a nodule or lung mass with no indication of reassessment by CT scan before the next round of screening, as recommended by the multidisciplinary consultation meeting OR CI2b- Person not eligible for screening with a nodule or lung mass with an indication for reassessment by CT scan without immediate diagnostic workup (PET scan, biopsy, surgery) as determined by the multidisciplinary consultation meeting.
- Group B CI1- Age \> 18 years AND CI2- Indication for biopsy or surgical excision for diagnostic and therapeutic purposes proposed in a multidisciplinary consultation meeting.
- Group C CI1a- Age 40 - 75 and daily smoking for at least 20 years initiated before age 15 OR CI1b- Age 50 - 75 and passive smoking for at least 20 years in a closed environment (family or workplace) OR CI1c- Age 50 - 75 and smoking 10 cig/d for 30 years or 15 cig/d for 25 years or 20 pack-years with no withdrawal period OR
- CI1d- Age 50 - 75 and daily smoking for at least 10 years combined with at least one other lung cancer risk factor from among :
- Self-reported daily passive smoking for \> 10 years (smokers at home or in enclosed environments)
- Self-reported exposure to a lung carcinogen: Radon, coal smoke, soot, diesel, nickel, beryllium, arsenic, cadmium, asbestos
- 1st-degree family history of lung cancer
- Personal history of tobacco-related disease, including atheromatous cardiovascular disease, COPD or emphysema, cancer not monitored by chest imaging
- weekly use of cannabis (joints) for 10 years
- All Groups:
- Have signed an informed consent form
- Affiliated with or benefiting from a social security scheme
- Male or female
Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.