Status:

ACTIVE_NOT_RECRUITING

Analysis of Specimens From Individuals With Pulmonary Fibrosis

Lead Sponsor:

National Human Genome Research Institute (NHGRI)

Conditions:

Pulmonary Fibrosis

Healthy Volunteers

Eligibility:

All Genders

18-115 years

Brief Summary

The etiology of pulmonary fibrosis is unknown. Analyses of blood, genomic DNA, and specimens procured by bronchoscopy, lung biopsy, lung transplantation, clinically-indicated extra-pulmonary biopsies,...

Detailed Description

The etiology of pulmonary fibrosis is unknown. Analyses of blood, genomic DNA, and specimens procured by bronchoscopy, lung biopsy, lung transplantation, clinically-indicated extra-pulmonary biopsies,...

Eligibility Criteria

Inclusion

  • INCLUSION CRITERIA:
  • Individuals who are 18 years of age or older with any of the following:
  • Idiopathic pulmonary fibrosis \[defined by the American Thoracic Society/European Respiratory Society guidelines\],
  • Familial pulmonary fibrosis \[defined as idiopathic pulmonary fibrosis in two or more first-degree relatives\],
  • Relatives of patients with hereditary pulmonary fibrosis,
  • Hermansky-Pudlak syndrome (diagnosed by paucity or deficiency of platelet dense bodies on whole mount electron microscopy or by genetic testing),
  • Pulmonary fibrosis associated with collagen vascular diseases or autoinflammatory disorders,
  • Pulmonary fibrosis post-COVID-19 \[i.e., pulmonary fibrosis in an individual recovering from SARS-CoV-2 infection\], or
  • Healthy research volunteers by history and indicated tests (individuals without history of chronic pulmonary disorder, collagen vascular disease, or bleeding disorder).
  • EXCLUSION CRITERIA:
  • Individuals with any of the following:
  • Significant inhalational exposure to fibrogenic fibers or dusts or exposure to drugs associated with pulmonary fibrosis,
  • Uncontrolled ischemic heart disease,
  • Uncorrectable bleeding diathesis,
  • Pregnancy or lactation (excluded due to exposure of unnecessary risks), or
  • Inability to give informed consent (excluded due to exposure of unnecessary risks).

Exclusion

    Key Trial Info

    Start Date :

    June 9 2004

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ACTUAL

    End Date :

    Estimated Enrollment :

    315 Patients enrolled

    Trial Details

    Trial ID

    NCT00084305

    Start Date

    June 9 2004

    Last Update

    January 5 2026

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    National Institutes of Health Clinical Center

    Bethesda, Maryland, United States, 20892