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Clinical Trial Summary

In this protocol, the investigators are examining the use of a novel pathogen testing technology and method of identification of antibiotic susceptibility against the conventional C & S testing for patients with both complicated and uncomplicated UTIs. The investigators will examine the two modes in terms of objective patient related outcomes, i.e. 1) diagnostic accuracy and degree of detail of final analysis; 2) time to resolution of symptoms; 3) quality of life as defined by particularly symptomology and "bothersomeness" of the symptoms; and 4) overall cost.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02623179
Study type Interventional
Source Southwest Regional PCR, LLC
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Status Completed
Phase N/A
Start date January 15, 2016
Completion date December 31, 2016