Clin2
NCT06702228Possibly a fitRecruiting

Precision care for pulmonary fibrosis in Ireland

Connective Tissue DiseasesInterstitial Lung DiseaseIdiopathic Pulmonary FibrosisFamilial Idiopathic Pulmonary FibrosisPulmonary FibrosisPulmonary Fibrosis Interstitial

Part of Genetic & congenital, Lungs & breathing, Skin clinical trials.

This trial is for people with scarring lung disease (pulmonary fibrosis) in Ireland. It aims to better understand and care for the condition, especially in families. The study will look at medical data and may help improve diagnosis and treatment.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
300 people
Ages
18 years to 85 years
Study type
Observational

Who can take part

  • You must have a type of scarring lung disease (fibrotic ILD) diagnosed by a team of doctors.
  • Your lung disease must fall into one of these groups: (a) you have a blood relative with scarring lung disease, (b) you have IPF (a specific type) without a family history, or (c) you have a connective tissue disease like rheumatoid arthritis, scleroderma, Sjogren's, myositis, or lupus.
  • You must be willing to give written permission to join the study.
  • You cannot be in another clinical trial that tests a treatment right now.
  • Your lung scarring should not be caused by an allergy (like mold or birds) or by asbestos exposure.
  • Your doctor must expect you to live longer than 12 months, based on your overall health.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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