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Clinical Trials/NCT02305342
NCT02305342
Completed
Not Applicable

Antibiotic Susceptibility of Bacterial Uro-Pathogens In Patients Attending Family Physicians" (In Vitro Study)

Abbott1 site in 1 country350 target enrollmentNovember 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Urinary Tract Infections (UTIs)
Sponsor
Abbott
Enrollment
350
Locations
1
Primary Endpoint
Sensitivity of Uropathogens
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

This study is aiming to evaluate the sensitivity of uropathogens isolated in patients with community acquired UTI with Enoxacin in comparison to other antimicrobials. While Secondary objective is to study the spectrum of uropathogens responsible for community acquired UTI in local population

Detailed Description

Mid stream , clean catch urine specimens of patients with uncomplicated community acquired UTI sent to microbiology labs by treating consultants from filter clinics for evaluation of pathogens will be utilized for sensitivity analysis. Only the first positive urine culture obtained per sample will be included in the analysis to eliminate any possibility of recurrence and nosocomial infection. The polymicrobial cultures and cultures with multidrug-resistant uropathogens will not be included in the analysis. Cultures with common contaminants, including coagulase-negative staphylococci and hemolytic streptococci, and cultures with Candida growth will be excluded. . Data points to be collected will be date of collection, computer generated Lab #, age, gender,list of cultured organisms, sensitivity of organisms with antibiotics.

Registry
clinicaltrials.gov
Start Date
November 2014
End Date
February 2015
Last Updated
11 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Abbott
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Samples from primary care clinics from patients who reports UTI symptoms and in which uropathogens are isolated will be included.

Exclusion Criteria

  • Samples from specialized, hospitalized or catheterized patients.

Outcomes

Primary Outcomes

Sensitivity of Uropathogens

Time Frame: 3 months

Sensitivity of identified organisms shall be noted by the zone size in millimeters of the cultured organisms. "Sensitive", "Intermediate" and "Resistant" labels shall be used as per Clinical Laboratory Standard Institute (CLSI) guidelines.

Secondary Outcomes

  • Common UTI pathogens(3 months)

Study Sites (1)

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