Actively Recruiting

Age: 18Years +
All Genders
ID06235645

Detection of Rheumatoid Arthritis-Interstitial Lung Disease by Thoracic Ultrasound

Led by University Hospital, Tours · Updated on 2026-04-30

280

Participants Needed

1

Research Sites

17 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Rheumatoid arthritis (RA) is an autoimmune disease that can affect various organs, including the lungs, leading to rheumatoid arthritis-interstitial lung disease (RA-ILD), which increases mortality among RA patients. The prevalence of RA-ILD varies depending on the screening method used. While chest CT is the current gold standard for detecting RA-ILD, it is costly, time-consuming, and involves radiation exposure. Lung ultrasound (LUS) is emerging as a quicker, non-irradiating, and less expensive tool for detecting lung damage and is being evaluated as a screening method for RA-ILD in patients at risk. This observational study involves patients with RA who have risk factors for RA-ILD and are regularly reassessed in a rheumatology day hospital. Eligible patients who have had chest CT and pulmonary function tests (PFT) within six months before or after their follow-up visit will be invited to participate. LUS examinations will be conducted by experienced operators using a linear probe to explore 14 intercostal spaces, with findings compared to chest CT results. Participation does not change usual follow-up care. Participants will undergo lung ultrasound and chest CT scans as part of their routine care, with lung ultrasound results recorded and anonymized. The study will measure the sensitivity and specificity of thoracic ultrasound compared to chest CT over two years. Researchers will also evaluate ultrasound signs such as B lines, pleural line thickening, and pleural line irregularity. The study aims to clarify the usefulness of LUS as a screening tool for RA-ILD while monitoring safety and effectiveness during regular clinical visits.

CONDITIONS

Brief Title

dEtection of rheumAtoid aRthritis - Interstitial Lung dIseasE by Thoracic ultRasound

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patient (age > 18 years) followed at CHU of Tours
  • Diagnosis of rheumatoid arthritis validated according to ACR 2010 criteria or EULAR classification
  • Patient who has had or will have a thoracic CT scan and pulmonary function tests within 6 months before or after inclusion
  • Patient with at least two risk factors for developing RA-ILD including: male sex, active or former smoker with 20 pack-years or more, age over 60 years, elevated rheumatoid factor or anti-CCP antibodies, or high RA activity score (DAS28 > 3.2)
Not Eligible

You will not qualify if you...

  • Diagnosis of congenital lung disease
  • Diagnosis of another autoimmune disease associated with RA linked to ILD (such as systemic sclerosis, myositis, dermatomyositis, mixed connective tissue disease, systemic lupus erythematosus, or ANCA vasculitis), except for secondary Gougerot-Sjögren's syndrome
  • Current or past lung cancer
  • History of thoracic irradiation
  • Thoracic transplant recipients
  • Previous invasive thoracic procedures
  • Diseases causing pleural thickening like silicosis, asbestosis, known pleural plaque, or pleural sequelae of tuberculosis
  • Pregnant or breastfeeding women
  • Patients under legal protection such as guardianship or curatorship
  • Patients who object to data processing
  • Current or recent (within one month) lung infection
  • Presence of liquid or gaseous pleural effusion

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Within 6 months before or after inclusion

Participants undergo thoracic ultrasound performed by an experienced operator to evaluate signs of rheumatoid arthritis-associated interstitial lung disease, alongside chest CT and pulmonary function tests as part of routine care.

1 visit (in-person) for ultrasound evaluation

Long-term Monitoring

Duration - 2 years

Participants who undergo routine rheumatology follow-up are observed to assess the sensitivity and specificity of thoracic ultrasound compared to chest CT over 2 years.

Trial Site Locations

Total: 1 location

1

university hospital Tours

Tours, France, 37000

Actively Recruiting

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Research Team

S

Sylvie LEGUE

A

Ariane MERLIN-DOMONT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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Published Research Related To This Trial

A population-based cohort study of rheumatoid arthritis-associated interstitial lung disease: comorbidity and mortality.

Charlotte Hyldgaard, Ole Hilberg, Alma Becic Pedersen...

https://pubmed.ncbi.nlm.nih.gov/28611082

Incidence and mortality of interstitial lung disease in rheumatoid arthritis: a population-based study.

Tim Bongartz, Carlotta Nannini, Yimy F Medina-Velasquez...

https://pubmed.ncbi.nlm.nih.gov/20155830

Fibrosing alveolitis in patients with rheumatoid arthritis as assessed by high resolution computed tomography, chest radiography, and pulmonary function tests.

J K Dawson, H E Fewins, J Desmond...

https://pubmed.ncbi.nlm.nih.gov/11462065

Two sides of the same coin? A review of the similarities and differences between idiopathic pulmonary fibrosis and rheumatoid arthritis-associated interstitial lung disease.

Scott Matson, Joyce Lee, Oliver Eickelberg

https://pubmed.ncbi.nlm.nih.gov/33303554

Baseline Characteristics and Progression of a Spectrum of Interstitial Lung Abnormalities and Disease in Rheumatoid Arthritis.

Leticia Kawano-Dourado, Tracy J Doyle, Karina Bonfiglioli...

https://pubmed.ncbi.nlm.nih.gov/32428513