Cohort of IPF Patients Experiencing an Exacerbation

University Hospital, Gentofte, Copenhagen

Status: Enrolling

Conditions: Idiopathic Pulmonary Fibrosis

Study type: Observational

Funder types: Other

Identifiers

NCT04442711

PFBIO-EXA

Details and patient eligibility

About

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.

Full description

The aim of this study is to investigate the diagnostic and prognostic value of clinical and 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.

Enrollment: 50 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

50 participants in 1 patient group

PFBIO-EXA

Description:

All patients recruited for PFBIO-EXA from the original PFBIO cohort are included into the cohort.