Cohort of IPF Patients Experiencing an Exacerbation

  • STATUS
    Recruiting
  • End date
    Jun 1, 2025
  • participants needed
    50
  • sponsor
    University Hospital, Gentofte, Copenhagen
Updated on 19 February 2024
fibrosis
pulmonary fibrosis

Summary

Extension of the PFBIO cohort which includes patients with newly diagnosed idiopathic pulmonary fibrosis (IPF) for longitudinal follow-up for up to 5 years.

In the PFBIO-EXA extension, patients are included if they experience an exacerbation, or other increase in respiratory symptoms requiring hospital admission, for further collection of clinical and biological data.

Description

The aim of this study is to investigate the diagnostic and prognostic value of blood biomarkers during exacerbations, or other increase in respiratory symptoms requiring hospital admission in patients with IPF.

Patients that are already included in the PFBIO-cohort (NCT02755441) and who are admitted to hospital with an increase in respiratory symptoms, are also included in PFBIO-EXA.

Patients are recruited within 24 hrs. from hospital admission with respiratory worsening, where clinical data, and blood samples are collected. The blood samples are investigated for the same blood biomarkers as PFBIO.

Patient related outcomes are also collected, including quality-of-life questionnaires and outcomes of the exacerbations.

Details
Condition Pulmonary Fibrosis, Pulmonary Fibrosis, Idiopathic Pulmonary Fibrosis, Idiopathic Pulmonary Fibrosis
Age 18-100 years
Clinical Study IdentifierNCT04442711
SponsorUniversity Hospital, Gentofte, Copenhagen
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Admitted with an increase in respiratory symptoms
Already included in PFBIO or included simultaneously in PFBIO and PFBIO-EXA
Age at least 18 years

Exclusion Criteria

Unable to provide informed consent
Clear my responses

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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