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Pathogen Detection and Community Acquired Pneumonia

Community Acquired Pneumonia Clinical Trial

Official title:
Projected Influence of Enhanced Pathogen Detection on the Clinical Management of Community-Acquired Pneumonia

Clinical Trial Summary

Study to compare the number of community-acquired pneumonia (CAP) pathogens detected using current diagnostic tests to the number detected using the BioFire Diagnostics investigational polymerase chain reaction (PCR) platform.

Clinical Trial Description

Patients diagnosed in the emergency department with CAP that requires hospitalization provide a sputum sample for culture and sensitivity testing, urine for detection of S. pneumonia and L. pneumophila, an anterior nasal swab for S. aureus PCR, a nasopharyngeal swab for S. pneumonia PCR and the FilmArray LRTI v.2.0 IUO Panel, and blood for procalcitonin testing and, in cases in which the patient is suffering rigors and hypotension, cultures. As part of this study, sputum or sputum equivalent will be acquired for testing using the FilmArray LRTI v.2.0 IUO Panel. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02880384
Study type Interventional
Source Providence Health & Services
Contact
Status Completed
Phase N/A
Start date January 2017
Completion date December 20, 2020
View Details
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