NCT06956040Recruiting
Involvement of General Practitioners in Lung Cancer Screening
Source: ClinicalTrials.gov · Last updated 20 Nov 2025
Brief summary (registry, in English)
The main objective is to evaluate the adherence of smoking patients to lung cancer screening by low-dose CT scan, when proposed by the general practitioner.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 500 (estimated)
- First submitted
- 25 Apr 2025
- Start date
- 2 Jun 2025
- Primary completion date
- Dec 2027
- Lead sponsor
- Assistance Publique - Hôpitaux de Paris
- Diseases
- Lung cancer
- NCT number
- NCT06956040
What you commit to
- Study type: Interventional
- Planned participants: 500
- From 2 Jun 2025 to the primary completion date, Dec 2027
- 1 site in 1 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
- Thoracic CT scan performed within the previous year
- Inability to give free written informed consent prior to study participation
Other illness
- History of lung cancer
- People with severe co-morbidities contraindicating exploration and/or management of lung cancers
- People with a history of cancer under active surveillance by thoracic computed tomography (CT and PET scans)
- Recent weight loss, altered general condition or hemoptysis, raising suspicion of progressive lung cancer
- Signs of respiratory infection (fever, productive cough)
Other
- 1-year follow-up not possible
- Inability to travel independently to Hôpital Cochin or Hôpital Bichat for scans
- People in poor general health (=PS2 and above)
- People with rest dyspnea (=mMRC4)
- Patients under guardianship, curatorship or protected adults
Who the study is looking for
- Adults aged 50-74
- Active smoker or weaned smoker for less than 15 years, of at least 20 pack-years
- Affiliation with a social security scheme or CMU (beneficiary or beneficiary entitled)
- Written informed consent prior to study participation
Age in the registry: 50 years to 74 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hôpital Cochin Coordinator of this site? Confirm its status | Paris | France | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.