Actively Recruiting

Age: 18Years +
All Genders
NCT07457502

Domestic Environmental Exposure and Progression of ILD: An Exploratory Case-Control Study

Led by Ville de Paris · Updated on 2026-03-09

100

Participants Needed

2

Research Sites

182 weeks

Total Duration

On this page

Sponsors

V

Ville de Paris

Lead Sponsor

I

Institut National de la Santé Et de la Recherche Médicale, France

Collaborating Sponsor

AI-Summary

What this Trial Is About

The project titled "Domestic Environmental Exposure and Progression of Progressive or Stable Fibrosing Interstitial Lung Diseases: An Exploratory Case-Control Study" is a Category 3 study involving 60 patients with progressive or stable fibrosing interstitial lung diseases (ILDs). These patients are matched based on the same ILD subtype and their use or non-use of antifibrotic medication. The study aims to thoroughly describe the domestic environment of these patients and investigate the associations between the progression of pulmonary fibrosis and: i) The presence of pollutants and risk factors in the home, including concentrations of nitrogen dioxide, volatile organic compounds, aldehydes, fine particles, mold, dust mite allergens, building defects, and lifestyle habits that increase pollutant exposure. ii) The ambient air quality at the patients' addresses. Occupational exposures will also be considered in the analysis. This project is designed to enhance our understanding of how an unfavorable domestic environment impacts the progression of pulmonary fibrosis and to evaluate the effects of the CMEI (Comprehensive Environmental and Indoor Audit) on patients' ability to manage identified risk factors within their homes, their respiratory health, and their medical diagnosis. The CMEI audit is a preventive measure that could serve as a significant intervention to alter patient behavior, reduce exposure, and improve health outcomes. This project is sponsored by the Environmental Health Laboratories Department, in collaboration with Unit 1018 of the Research Center in Epidemiology and Population Health (CESP), and two investigative centers: Tenon Hospital and Paris Saint-Joseph Hospital.

CONDITIONS

Official Title

Domestic Environmental Exposure and Progression of ILD: An Exploratory Case-Control Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient aged over 18 years
  • Diagnosed with one of the following interstitial lung diseases: Idiopathic Pulmonary Fibrosis, Nonspecific Interstitial Pneumonia, Pneumoconioses, ILDs with autoimmune features, Pleuroparenchymal Fibroelastosis, Chronic Hypersensitivity Pneumonitis not primarily related to the home environment, Stage 4 fibrosing sarcoidosis, or unclassifiable ILDs
  • Has progressive fibrosis over the past 12 months (case group) or non-progressive fibrosis over the past 12 months (control group)
  • No reduction in ILD treatment in the 12 months before inclusion; patients without treatment may be included
  • Matched pairs with same ILD diagnosis and either both using or both not using antifibrotic treatment
  • Matched patients preferably within 3 months to limit seasonal lifestyle and housing differences
  • Has received information about the protocol and does not object to participation
  • Affiliated with or beneficiary of a social security scheme or universal health coverage
Not Eligible

You will not qualify if you...

  • Received CMEI advice within the past 12 months
  • Recently moved into current home less than 1 year ago
  • Lives less than 6 months per year in the home to be studied
  • Followed in psychiatry for a severe condition
  • Does not speak French and is not accompanied by a French-speaking person from the same home
  • Refuses to consent to participate
  • Does not live in Île-de-France
  • Has non-chronic Hypersensitivity Pneumonitis related to the domestic environment
  • Has sarcoidosis other than stage 4 fibrosing sarcoidosis
  • Adult under legal protection and unable to give consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 2 locations

1

Hôpital Paris Saint Joseph

Paris, Paris, France, 75014

Actively Recruiting

2

Hôpital de Tenon

Paris, Paris, France, 75020

Actively Recruiting

Loading map...

Research Team

V

Valerie BEX, 1

CONTACT

O

Oualid ALIOUI

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here