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Effectiveness of Probiotics Prophylaxis of Urinary Tract Infections in Children

Primary Purpose

Prevention of Urinary Tract Infections in Children

Status
Unknown status
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
Placebo control group
Probiotic experimental group
Sponsored by
Medical University of Warsaw
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Prevention of Urinary Tract Infections in Children focused on measuring Urinary Tract Infection, prophylaxis, probiotics

Eligibility Criteria

3 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Children's Hospital for The Medical University of Warsaw

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Placebo supply for 90 days

Probiotic supply for 90 days

Arm Description

Patients will receive placebo (in blinded sachets)

Patients will receive probiotics containing Lactobacillus rhamnosus PL1 and Lactobacillus plantarum PM1 (in blinded sachets).

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

frequencies of hospitalization due to UTI
the number of days of antibiotic therapy due to UTI

Full Information

First Posted
February 28, 2018
Last Updated
March 9, 2018
Sponsor
Medical University of Warsaw
Collaborators
Miralex Sp. z o.o.
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1. Study Identification

Unique Protocol Identification Number
NCT03462160
Brief Title
Effectiveness of Probiotics Prophylaxis of Urinary Tract Infections in Children
Official Title
Effectiveness of Prophylaxis of Urinary Tract Infections in Children With a Probiotic Containing Lactobacillus Rhamnosus PL1 and Lactobacillus Plantarum PM1, a Randomised Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2018
Overall Recruitment Status
Unknown status
Study Start Date
April 1, 2018 (Anticipated)
Primary Completion Date
April 1, 2019 (Anticipated)
Study Completion Date
September 1, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Medical University of Warsaw
Collaborators
Miralex Sp. z o.o.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prevention of Urinary Tract Infections in Children
Keywords
Urinary Tract Infection, prophylaxis, probiotics

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
106 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Placebo supply for 90 days
Arm Type
Placebo Comparator
Arm Description
Patients will receive placebo (in blinded sachets)
Arm Title
Probiotic supply for 90 days
Arm Type
Experimental
Arm Description
Patients will receive probiotics containing Lactobacillus rhamnosus PL1 and Lactobacillus plantarum PM1 (in blinded sachets).
Intervention Type
Other
Intervention Name(s)
Placebo control group
Intervention Description
Placebo will be administered orally, after dissolving the sachet in lukewarm water, every evening during the meal. The placebo appearance will be similar to the probiotic.
Intervention Type
Dietary Supplement
Intervention Name(s)
Probiotic experimental group
Intervention Description
Probiotic UroLact containing Lactobacillus rhamnosus PL1 and Lactobacillus plantarum PM1 will be administered orally, after dissolving the sachet in lukewarm water, every evening during the meal.
Primary Outcome Measure Information:
Title
frequencies of recurrence of UTI
Description
New onset of symptomatic UTI within the 6 months follow-up period.
Time Frame
6 months after intervention
Secondary Outcome Measure Information:
Title
frequencies of hospitalization due to UTI
Time Frame
6 months after intervention
Title
the number of days of antibiotic therapy due to UTI
Time Frame
6 months after intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Maria Daniel, MD
Phone
696477117
Ext
0048
Email
maria.daniel@wum.edu.pl
First Name & Middle Initial & Last Name or Official Title & Degree
Hanna Szymanik-Grzelak, PhD
Phone
223179656
Ext
0048
Email
h.szymanik@interia.pl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Malgorzata Panczyk-Tomaszewska, Assistant Professor
Organizational Affiliation
Medical University of Warsaw
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Maria Daniel, MD
Organizational Affiliation
Medical University of Warsaw
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Hanna Szymanik-Grzelak, PhD
Organizational Affiliation
Medical University of Warsaw
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Hospital for The Medical University of Warsaw
City
Warsaw
ZIP/Postal Code
02-091
Country
Poland

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
26140267
Citation
Tewary K, Narchi H. Recurrent urinary tract infections in children: Preventive interventions other than prophylactic antibiotics. World J Methodol. 2015 Jun 26;5(2):13-9. doi: 10.5662/wjm.v5.i2.13. eCollection 2015 Jun 26.
Results Reference
result
PubMed Identifier
26695595
Citation
Schwenger EM, Tejani AM, Loewen PS. Probiotics for preventing urinary tract infections in adults and children. Cochrane Database Syst Rev. 2015 Dec 23;2015(12):CD008772. doi: 10.1002/14651858.CD008772.pub2.
Results Reference
result
PubMed Identifier
29102297
Citation
Hosseini M, Yousefifard M, Ataei N, Oraii A, Mirzay Razaz J, Izadi A. The efficacy of probiotics in prevention of urinary tract infection in children: A systematic review and meta-analysis. J Pediatr Urol. 2017 Dec;13(6):581-591. doi: 10.1016/j.jpurol.2017.08.018. Epub 2017 Oct 9.
Results Reference
result
PubMed Identifier
33097017
Citation
Daniel M, Szymanik-Grzelak H, Turczyn A, Panczyk-Tomaszewska M. Lactobacillus rhamnosus PL1 and Lactobacillus plantarum PM1 versus placebo as a prophylaxis for recurrence urinary tract infections in children: a study protocol for a randomised controlled trial. BMC Urol. 2020 Oct 23;20(1):168. doi: 10.1186/s12894-020-00723-1.
Results Reference
derived

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Effectiveness of Probiotics Prophylaxis of Urinary Tract Infections in Children

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