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Recruiting NCT03478553

The Genetics of Pulmonary Fibrosis

Observational Idiopathic Pulmonary Fibrosis (IPF)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Blood draw, Questionnaire.
Who it may be relevant to
Registry conditions: Idiopathic Pulmonary Fibrosis (IPF). Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Idiopathic Pulmonary Fibrosis, a Disease Initiated by Mucociliary Dysfunction

Overview

This study seeks to screen first degree family members of people with Idiopathic Pulmonary Fibrosis (IPF) for the earliest signs of lung fibrosis.

Detailed description

The purpose of this study is to explore genetic factors associated with the development of pulmonary fibrosis. The investigators aim is to identify and explore genetic loci that affect development of pulmonary fibrosis and also explore related environmental exposures. Idiopathic pulmonary fibrosis (IPF) is one of the interstitial lung diseases under the broader umbrella of idiopathic interstitial pneumonias (IIP). The investigators hypothesize that inherited genetic factors are associated with pulmonary fibrosis. To investigate the genetics of pulmonary fibrosis, the investigators plan to enroll individuals with pulmonary fibrosis and their family members.

Interventions

  • Other Blood draw
    Blood draw
  • Other Questionnaire
    Pulmonary Fibrosis Questionnaire

Primary outcome measures

  • Identify and explore genetic loci and related environmental exposures in individuals with familial pulmonary fibrosis and their relatives. [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

  • Age at least 18 years old
  • Family member diagnosed with IPF

Exclusion criteria

\- No family member with IPF

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Family-based

Study locations

United States · 1 center
  • University of Colorado Anschutz Medical Campus — Aurora

Identifiers

NCT: NCT03478553 · 15-1147 · W81XWH-17-1-0597_1a

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗