Actively Recruiting

Phase Not Applicable
Age: 50Years - 74Years
All Genders
NCT06956040

Involvement of General Practitioners in Lung Cancer Screening

Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-11-20

500

Participants Needed

1

Research Sites

130 weeks

Total Duration

On this page

Sponsors

A

Assistance Publique - Hôpitaux de Paris

Lead Sponsor

U

URC-CIC Paris Descartes Necker Cochin

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Involvement of General Practitioners in Lung Cancer Screening

Who Can Participate

Age: 50Years - 74Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 50-74
  • Active smoker or ex-smoker who quit less than 15 years ago
  • Smoking history of at least 20 pack-years
  • Affiliated with a social security scheme or CMU
  • Able to provide written informed consent before participating
Not Eligible

You will not qualify if you...

  • History of lung cancer
  • Thoracic CT scan done within the last year
  • Unable to commit to a 1-year follow-up
  • Unable to travel independently to Hôpital Cochin or Hôpital Bichat for scans
  • Severe health issues preventing lung cancer exploration or treatment
  • Poor general health status (performance status 2 or higher)
  • Active cancer surveillance involving thoracic CT or PET scans
  • Severe resting breathlessness (mMRC 4)
  • Recent weight loss, poor general condition, or coughing up blood suggesting progressive lung cancer
  • Signs of respiratory infection such as fever or productive cough
  • Under legal guardianship or unable to provide free written informed consent

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Hôpital Cochin

Paris, France, 75014

Actively Recruiting

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Research Team

C

Céline BUFFEL du VAURE, PhD

CONTACT

A

Alice CAMARA, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

0

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