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NCT00258570Recruiting

Genetic Polymorphisms in Idiopathic Pulmonary Fibrosis (IPF)

Genetic Polymorphisms in Idiopathic Pulmonary Fibrosis

Source: ClinicalTrials.gov · Last updated 31 Aug 2026

Brief summary (registry, in English)

The purposes of this study are: * to determine if there are specific genetic traits that might explain why patients have developed pulmonary fibrosis; * to determine if specific genetic traits account for differing patterns of inflammation and scar tissue that has formed in the patient's lungs.

Status (registry)
Recruiting
Study type
Observational
Enrollment
2000 (estimated)
First submitted
23 Nov 2005
Start date
Jan 2003
Primary completion date
Jul 2035
Lead sponsor
University of Pittsburgh
NCT number
NCT00258570

What you commit to

  • Study type: Observational
  • Planned participants: 2000
  • From Jan 2003 to the primary completion date, Jul 2035
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Age

  • Under 18 years of age

Other

  • Non-fibrotic ILD

Who the study is looking for

  • 18 years of age or older
  • Diagnosis of pulmonary fibrosis confirmed by physical examination, pulmonary function testing, chest X-ray, and computed tomography (CT) scans.
  • Adult patients who are seeking treatment at the Dorothy P. and Richard P. Simmons Center for Interstitial Lung Disease.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Pittsburgh
Coordinator of this site? Confirm its status
PittsburghUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.