Structuring of a Lung Cancer Screening Program Including Clinical, Radiological and Biological Phenotyping Useful for the Development of Individualized Risk Prediction Tools: PREVALUNG ETOILE
NCT05649046 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 160
Last updated 2024-03-18
Summary
Patients treated at the Hôpital Nord de Marseille for at least one smoking-related pathology (atheroma, chronic bronchitis, non-progressive cancer \> 5 years) or with eligibility criteria for lung cancer screening (inclusion criteria in the NLST or NELSON studies or American recommendations) Interventional study with minimal risks and constraints, with evaluation of lung cancer prevalence; immunological, blood inflammatory and microbiota profile
Determine the maximum clinical, radiological, and biological phenotyping completeness rate following the implementation of a new lung cancer screening care pathway with multidimensional clinical, radiological, and biological phenotyping capabilities
Conditions
- Smoking-related Pathology
- Atheroma
- Chronic Bronchitis
- Non-progressive Cancer > 5 Years
- Lung Cancer
Interventions
- DEVICE
-
thoracic scan Low dose
within 3 months after the V0 visit
- BIOLOGICAL
-
BLOOD SAMPLE
within 3 months after the V0 visit
- BIOLOGICAL
-
FECES SAMPLE
within 3 months after the V0 visit
Sponsors & Collaborators
-
Assistance Publique Hopitaux De Marseille
lead OTHER
Principal Investigators
-
Emilie GARRIDO PRADALIE · ASSIATANCE PUBLIQUE HOPITAUX DE MARSEILLE
Study Design
- Allocation
- NA
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 45 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-01-23
- Primary Completion
- 2024-06-01
- Completion
- 2024-06-01
Countries
- France
Study Locations
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