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Clinical Trials/CTRI/2019/12/022486
CTRI/2019/12/022486Not yet recruitingNot Applicable

A clinical study of UTI caused by Multi-Drug Resistant (MDR) uropathogens in a tertiary care hospital

Not provided1 site in 1 country1,500 target enrollmentStarted: December 23, 2019Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
1,500
Locations
1
Primary Endpoint
1. MDR Uropathogens causing UTI

Study Overview

Brief Summary

Urinary Tract Infection (UTI) is a common bacterialinfection, which contributes to a frequent cause of morbidity in out-patientsas well as in hospitalized patients. There are numerous cases ofantimicrobial resistance to the commonly used antibiotics in the developed anddeveloping countries. Resistance to newer and more potent antimicrobialsare no exceptions, thereby making the therapeutic options very limited tocertain antimicrobial agents like carbapenem, colistin and fosfomycin. The updated knowledge and situation of the prevailing bacterial uropathogens thatare multidrug resistant (MDR) is of prime importance for the proper use ofantimicrobial drugs and also for policy making to combat multidrug resistancein UTIs. Antimicrobial resistance surveillance is necessary todetermine the size of the problem and to guide the empirical selection ofantimicrobial agents for treating infected patients. This study is aimed tostudy the profile of MDR uropathogens causing UTI in a tertiary care hospitaland assess their antimicrobial susceptibility pattern, clinical course andoutcome.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
0.00 Day(s) to 90.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • 1.Subjects whose urine sample when processed showed significant growth of one or more organisms.

Exclusion Criteria

  • 1.Subjects whose urine sample was contaminated.
  • 3.Subjects whose urine sample showed insignificant bacteriuria.

Outcomes

Primary Outcomes

1. MDR Uropathogens causing UTI

Time Frame: 6 months

Secondary Outcomes

  • 1. Antimicrobial susceptibility pattern(2. Clinical course and outcome)

Investigators

Sponsor
Not provided

Study Sites (1)

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