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Trial Title:
Adherence to Lung Cancer Screening by Low-dose Thoracic CT in Haut-Rhin Department, France.
NCT ID:
NCT06020443
Condition:
High-Risk Cancer
Lung Cancer
Conditions: Official terms:
Lung Neoplasms
Conditions: Keywords:
screening
low dose chest computed tomography
lung cancer
Study type:
Interventional
Study phase:
N/A
Overall status:
Recruiting
Study design:
Allocation:
N/A
Intervention model:
Single Group Assignment
Intervention model description:
Low Dose chest CT Scan for Lung Cancer Screening
Primary purpose:
Diagnostic
Masking:
None (Open Label)
Intervention:
Intervention type:
Procedure
Intervention name:
Low Dose chest CT Scan for Lung Cancer Screening
Description:
Low dose CT scans will be performed for three years
Arm group label:
Patients with a high risk of lung cancer
Summary:
The main objective of the study is to measure adherence to a lung cancer screening
program using low-dose thoracic CT.
Detailed description:
Secondary objectives
1. To evaluate patient compliance over the entire duration of the screening program
2. To assess patient smoking cessation
3. To describe radiation doses received during CT scans
4. To identify organizational constraints for general practitioners
5. To compare stages at diagnosis before and after implementation of screening program
Conduct of research Eligible patients will be identified by general practitioners.
Patients included will require a low-dose thoracic CT scan to be performed by a
radiologist of their choice. Smoking cessation will be systematically proposed, and will
be carried out by the general practitioner or a tobaccologist.
The radiation dose from thoracic CT scans should not exceed 100 mGy.cm Product Dose
Length (i.e. < 1.5 mSv). Imaging reports will be forwarded to the general practitioner.
If the first CT scan is negative (T0): a second scan will be scheduled 1 year later (T1).
If this second scan is also negative, in the absence of lung cancer risk factors other
than smoking, scans will then be performed every two years. In the presence of a risk
factor for lung cancer (other than tobacco), screening will remain annual.
In the event of a result classified as uncertain: a follow-up scan is scheduled at 3
months ; if the follow-up scan is negative, the next screening will be scheduled 1 year
after this follow-up scan. If the screening performed 1 year later is also negative,
subsequent screenings will be performed annually.
In the event of a positive result: the general practitioner will refer the patient to a
pneumologist of his/her choice for further examinations; data from these additional
examinations will be collected.
The screening protocol may evolve in line with recommendations issued by the French
National Authority for Health (HAS).
For participants undergoing CT scan at the imaging department of Emile Muller hospital in
Mulhouse (GHRMSA), a blood sample will be collected (optional) for subsequent biomarker
assays.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
- Patients aged 50 to 74 years
- Smoking OR having smoked (withdrawal of <15 years): ≥15 cigarettes/day for ≥25 years
OR ≥10 cigarettes/day for ≥30 years
- Affiliated or beneficiary of a social security scheme
- Written informed consent
Exclusion Criteria:
- Inability to walk up two flights of stairs without stopping
- BMI > 35 kg/m²
- Recent chest CT scan < 1 year
- Personal history of lung cancer < 5 years or under treatment
- Personal history of cancer being monitored by chest CT scan
- Contraindication to lung cancer treatment or diagnostic investigations
- Current or recent respiratory symptoms immediately suggestive of lung cancer
- Pregnant or breast-feeding woman
- Person under court protection, guardianship or curatorship
- Person deprived of liberty by judicial or administrative decision.
Gender:
All
Minimum age:
50 Years
Maximum age:
74 Years
Healthy volunteers:
No
Locations:
Facility:
Name:
Cabinet de médecine générale
Address:
City:
Colmar
Zip:
68000
Country:
France
Status:
Recruiting
Contact:
Last name:
Patrick Strentz
Start date:
November 6, 2023
Completion date:
November 2026
Lead sponsor:
Agency:
Groupe Hospitalier de la Region de Mulhouse et Sud Alsace
Agency class:
Other
Source:
Groupe Hospitalier de la Region de Mulhouse et Sud Alsace
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06020443