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Advancing Prevention of Pulmonary Fibrosis

Active, not recruiting
Conditions
IPF
Pulmonary Fibrosis
ILD
Interventions
Other: Sample collection
Other: Questionnaires
Radiation: High resolution CT scan of the chest
Diagnostic Test: Pulmonary Function Test
Registration Number
NCT04564183
Lead Sponsor
University of Colorado, Denver
Brief Summary

This study plans to learn more about pulmonary fibrosis and how it develops. We want to determine if the disease can be detected early, before the lung is permanently scarred.

This study will enroll participants who are not currently diagnosed with pulmonary fibrosis, but who have family members with pulmonary fibrosis. Because there is an increased risk within affected families, this cohort will allow us to learn how pulmonary fibrosis develops, and how the lungs change over time.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
800
Inclusion Criteria
  • Unaffected first degree relative from Familial Interstitial Pneumonia families (two or more family members with IIP)
  • Age at least 40 years old and younger than 75 years old
Read More
Exclusion Criteria
  • Diagnosed with known (physician-diagnosed) pulmonary fibrosis prior to informed consent
  • Other genetic diseases associated with interstitial lung disease
  • Pregnant women
Read More

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Full CohortSample collectionEntire study population
Full CohortQuestionnairesEntire study population
Full CohortPulmonary Function TestEntire study population
Full CohortHigh resolution CT scan of the chestEntire study population
Primary Outcome Measures
NameTimeMethod
Screen all subjects for early Idiopathic Pulmonary Fibrosis (IPF) with High Resolution CT Scan of the ChestBaseline

All subjects will be screened with a high resolution CT scan to identify early signs of lung fibrosis. CT scans will be evaluated by study radiologists.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Colorado Anschutz Medical Campus

🇺🇸

Aurora, Colorado, United States

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