An Adjunct Test Distinguishing Bacterial From Viral Etiology Improves Resource Utilization and Efficiency in the ED.

Recruiting N/A Interventional Study
Respiratory Tract Infections
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
100 (estimated)
Sponsor
The University of Texas Health Science Center, Houston · Other
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About This Trial

The purpose of this study is to evaluate overall changes in patient management and longer-term resource utilization between control and test arms, including (but not limited to) additional work-up (including other diagnostic tests and consults), antimicrobial treatments, disposition decisions and hospital length of stay (LOS)

Trial Locations
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Eligibility Criteria
Inclusion Criteria for main study population : * Current disease duration ≤ 7 days * Temperature ≥ 37.8°C (100°F) or tactile fever, noted at least once within the last 7 days * Clinical suspicion of bacterial or viral respiratory tract infection (RTI) Exclusion Criteria for main study population: …
Contacts

David Robinson, MD,MS,MMM

(713) 500-7873

David.J.Robinson@uth.tmc.edu

CONTACT

Neomi Sepulveda

713.500.8474

Neomi.Sepulveda@uth.tmc.edu

CONTACT