Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
50 participants
OBSERVATIONAL
2020-06-13
2028-12-31
Brief Summary
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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.
Detailed Description
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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.
Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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PFBIO-EXA
All patients recruited for PFBIO-EXA from the original PFBIO cohort are included into the cohort.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Already included in PFBIO or included simultaneously in PFBIO and PFBIO-EXA
* Age at least 18 years
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University Hospital, Gentofte, Copenhagen
OTHER
Responsible Party
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Nils Hoyer
Principal Investigator
Locations
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Herlev and Gentofte Hospital
Hellerup, Copenhagen, Denmark
Countries
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Facility Contacts
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Nils Hoyer, MD PhD
Role: primary
Other Identifiers
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PFBIO-EXA
Identifier Type: -
Identifier Source: org_study_id