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Pulmonary Fibrosis and Telomerase Mutation Study

NCT01501578 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 81

Last updated 2018-02-20

No results posted yet for this study

Summary

This study is an observational and retrospective study of patients with pulmonary fibrosis associated or not with telomerase mutation.

The purpose of this study is to describe in detail the cases with telomerase mutation in terms of features on CT scan, respiratory function and evolution, in comparison to control subjects with idiopathic pulmonary fibrosis and no telomerase mutation identified or family history.

Conditions

Sponsors & Collaborators

  • Bichat Hospital

    collaborator OTHER

  • Groupe d'Etudes et de Recherche sur les Maladies Orphelines Pulmonaires

    lead OTHER

Principal Investigators

  • vincent Cottin, MD · Hospices civils de Lyon / University Lyon I

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-12-31
Primary Completion
2012-06-30
Completion
2015-12-31

Countries

  • France

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01501578 on ClinicalTrials.gov