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Clinical Trials/NCT03462160
NCT03462160
Unknown
Not Applicable

Effectiveness of Prophylaxis of Urinary Tract Infections in Children With a Probiotic Containing Lactobacillus Rhamnosus PL1 and Lactobacillus Plantarum PM1, a Randomised Clinical Trial

Medical University of Warsaw1 site in 1 country106 target enrollmentApril 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prevention of Urinary Tract Infections in Children
Sponsor
Medical University of Warsaw
Enrollment
106
Locations
1
Primary Endpoint
frequencies of recurrence of UTI
Last Updated
8 years ago

Overview

Brief Summary

The investigators aim to assess the effectiveness of prophylaxis of urinary tract infections in children with a probiotic containing Lactobacillus rhamnosus PL1 and Lactobacillus plantarum PM1. It is formulated a hypothesis that a 3-months course of probiotic prophylasis is more effective than placebo.

Detailed Description

In previously published European and global guidelines, there has been no consensus among experts regarding the prophylaxis of recurrence urinary tract infections. Depending on the recommendation, the prevention of recurrence UTI should be used, not justified, or should be used in special cases. However, preparations that will be effective in preventing UTI and will not cause bacterial resistance are still sought. 106 patients aged 3 to 18 years with recurrence UTIs (defined as: ≥2 infections in the upper urinary tract or 1 UTI in the upper urinary tract and ≥1 in the lower urinary tract or ≥3 or more UTI in the lower urinary tract in one year) or children with ≥1 infection in the upper urinary tract and ≥1 of recurrent UTIs risk factors (congenital anomalies of the kidney and urinary tract, constipation, bladder dysfunction, myelomeningocele, sexual activity in girls) will be randomly assigned to receive a 90-days prophylaxsis arm (probiotic UroLact containing Lactobacillus Rhamnosus PL1 and Lactobacillus Plantarum PM1) or a 90-days placebo arms. The primary outcome measure will be frequencies of recurrence of UTI during the 6 months after the intervention.

Registry
clinicaltrials.gov
Start Date
April 1, 2018
End Date
September 1, 2019
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Medical University of Warsaw
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • recurrent UTIs (defined as: ≥2 infections in the upper urinary tract or 1 UTI in the upper urinary tract and ≥1 in the lower urinary tract or ≥3 or more UTI in the lower urinary tract in one year) OR 1 infection in the upper urinary tract and ≥1 of recurrent UTIs risk factors: congenital anomalies of the kidney and urinary tract, constipation, bladder dysfunction, myelomeningocele, sexual activity in girls
  • ≥1 episode of urinary tract infection in the last 6 months

Exclusion Criteria

  • intake of probiotic preparations for ≥1 month in the last 3 months
  • known allergy to the study products
  • immunosuppression therapy
  • disease with immune deficiency
  • children with other coexisting infection, e.g. meningitis, sepsis, pneumonia, otitis

Outcomes

Primary Outcomes

frequencies of recurrence of UTI

Time Frame: 6 months after intervention

New onset of symptomatic UTI within the 6 months follow-up period.

Secondary Outcomes

  • frequencies of hospitalization due to UTI(6 months after intervention)
  • the number of days of antibiotic therapy due to UTI(6 months after intervention)

Study Sites (1)

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