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Rheumatoid Arthritis-associated Interstitial Lung Disease Definition (RAID)

U

University Hospital Center (CHU) of Liege

Status

Enrolling

Conditions

Rheumatoid Arthritis-Associated Interstitial Lung Disease

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT06184893
2022/52

Details and patient eligibility

About

This is a prospective multicenter study in southern Belgium to determine the prevalence and incidence of interstitial lung disease in patients with rheumatoid arthritis (RA).

Full description

This is a prospective multi-centric longitudinal study of the prevalence and incidence of pulmonary diseases in patients with RA.

During one year, patients with a RA diagnosis (according to the criteria of the American Society of Rheumatology) in the south of Belgium will be enrolled on a voluntary basis. If available, data including quality of life and symptoms questionnaires, medical examinations, 6-minute walk-tests, pulmonary function tests and chest CT will be collected during two years.

Furthermore, patients could be included (if available data) in two additional sub-cohorts:

  • "RAIDbio" sub-cohort studying biomarkers: volatile organic compounds, induced sputum and blood biomarkers;
  • "RAIDomix" sub-cohort studying radiomic patterns (based on high resolution computed tomography of the chest).

Due to a non-specific and poor clinical expression at beginning, there is currently an under-diagnosis of rheumatoid arthritis associated-interstitial lung disease (RA-ILD) at an early stage and we assume that an annual pneumological follow-up, search of early biomarkers and a radiomic approach of RA patients will overcome this issue. This should lead to a better follow-up and management (including the use of anti-fibrotic therapies in the future) of these patients and ultimately to a decrease in morbidity and mortality.

Enrollment

250 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Diagnosis of rheumatoid arthritis according to the criteria of the American Society of Rheumatology
  • Age > 18 years
  • Willing to participate in the study and sign the informed consent form (ICF) of participants or their legal authorized representative
  • RAIDbio subcohort : available data for one of the following analysis of biomarkers: volatile organic compounds, induced sputum or blood markers
  • RAIDomix : available data for high resolution computed tomography of the chest

Exclusion Criteria: none

Trial design

250 participants in 3 patient groups

General cohort
RAIDbio
Description:
Sub-cohort studying biomarkers: volatile organic compounds, induced sputum and blood biomarkers
RAIDomix
Description:
Sub-cohort studying radiomic patterns (based on high resolution computed tomography of the chest)

Trial contacts and locations

1

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Central trial contact

Anna Denis, MD; Julien Guiot, PhD

Data sourced from clinicaltrials.gov

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