Actively Recruiting

Phase Not Applicable
Age: 55Years - 74Years
All Genders
NCT06825078

Performance of Lung MRI Combined to Synthetic CT in the Follow-up of Lung Nodules

Led by University Hospital, Bordeaux · Updated on 2025-02-19

50

Participants Needed

1

Research Sites

102 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Lung cancer screening trials using low-dose chest CT scans have shown a significant reduction of cancer related mortality in subjects at high risk of lung cancer. However, high rate of false positives and overdiagnosis have led to invasive methods, which are not without risks. Evaluation of lung nodules using lung MRI with ultra short echo time sequences (UTE) has been found comparable to chest CT scans. Moreover, MRI has the advantage of multiparametric characterization of lesions using different tissue contrasts. Following the recommendation of the French National Authority for Health (HAS) to evaluate new methods of lung cancer screening, this prospective single center pilot study is designed to evaluate the performance of multiparametric lung MRI combined to synthetic CT in the diagnosis of lung cancer in heavily smokers or ex-smokers professionally exposed to carcinogens

CONDITIONS

Official Title

Performance of Lung MRI Combined to Synthetic CT in the Follow-up of Lung Nodules

Who Can Participate

Age: 55Years - 74Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Subject aged between 55 and 74 years
  • High risk of developing lung cancer due to exposure to lung carcinogens and smoking (30 pack-years or cessation less than 15 years)
  • Presence of at least one solid lung nodule 5 mm or larger on the initial scan
  • Ability and willingness to complete all scheduled visits and assessments
  • Subject has health insurance
  • Signed informed consent
Not Eligible

You will not qualify if you...

  • Signs of lung cancer
  • History of lung cancer
  • Severe life-threatening comorbidities within 6 months (recent stroke or advanced cancer discovery)
  • Chest scan performed less than one year ago
  • No exposure to occupational lung carcinogens as defined
  • No or insufficient tobacco exposure or cessation more than 15 years ago
  • Contraindications to MRI (pacemaker, implants, claustrophobia)
  • Pregnant or breastfeeding women
  • Poor understanding of French
  • Subject under legal protection

AI-Screening

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Trial Site Locations

Total: 1 location

1

CHU Bordeaux

Pessac, France

Actively Recruiting

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Research Team

I

Ilyes Benlala, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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