Recruiting
Phase 1
Phase 2

Probiotics

Sponsor:

London Health Sciences Centre

Code:

NCT02044965

Conditions

Urinary Tract Infection

Eligibility Criteria

Sex: All

Age: 12 - 17

Healthy Volunteers: Not accepted

Interventions

Antibiotic

Probiotic

Study Details

Brief summary:

Although clean intermittent catheterization (CIC) remains the mainstay to ensure complete low-pressure bladder emptying in neurogenic bladder (NB) patients, this forms a vehicle for bacterial entry and colonization of the urinary tract, which can lead to recurrent urinary tract infection (RUTI) and renal damage. Up to 25% of NB patients on CIC suffer from RUTI and daily, low-dose antibiotic prophylaxis is widely prescribed to prevent these infections. Unfortunately, this therapeutic option is not evidence-based and can be associated with a higher risk of RUTI secondary to development of antibiotic resistance. In addition, many children suffer from a range of adverse reactions and emergence of drug resistant organisms. Moreover, recent studies have shown that antibiotics cause a major disruption in the human microbiome, potentially leading to long term major problems.

Probiotics are live microorganisms, which when administered in adequate amounts confer a health benefit on the host. There is evidence that probiotics restore microbial homeostasis in the vagina, reduce the risk of pathogen ascension into the bladder, and modulate immunity to better protect the host. Probiotic strains, including Lactobacillus rhamnosus GR-1, Lactobacillus reuteri B-54 and RC-14, have been shown to be safe and efficacious in an oral formulation or as a vaginal suppository in improving the microbiota profile of the vagina and decreasing the risk of RUTI. Various mechanisms appear to be involved, including modulating antimicrobial and inflammatory defenses, up-regulating protective mucin production and reducing the pressure on pathogens to acquire antibiotic resistance genes. A randomized trial comparing probiotics to antibiotic prophylaxis in children with vesicoureteric reflux showed equivalent reduction in the incidence of RUTI and development of new renal scarring. In addition, down regulation of inflammatory cytokines can potentially favorably alter bladder function and prevent bladder fibrosis.

Investigators at London Health Sciences Centre (LHSC) have the opportunity to acquire clinical data that would strengthen the case for probiotics to be integrated into pediatric urology practice for managing CIC and RUTI. This would be the first such study in pediatric NB patients.

The main objective of this study is to determine whether the use of probiotics (lactobacilli) can decrease the impact of adverse side effects and the antibiotic resistance that is seen with the prolonged use of antibiotics for patients with neurogenic bladder conditions.

Conditions

Urinary Tract Infection

Study ID

NCT02044965

Start date

Jan, 2015

Status verified date

Sep, 2021

Completion date

Dec, 2023

Anticipated

Primary completion date

Dec, 2022

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 12 - 17

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • - Patients will have had a history of recurrent urinary tract infections over the past 12 months.
  • Patients will have been receiving chemoprophylaxis for at least one month.
  • Patients who are using clean intermittent catheterization to manage a neurogenic bladder condition.
  • PATIENTS WILL BE BETWEEN THE AGES OF 6-20.

Exclusion Criteria:

  • Patient has a known allergy to Septra
  • Patients pregnant or nursing will be excluded.

Study Design

Enrollment

36 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Prevention

Interventions and Outcome Measures

Arms

no intervention: Antibiotic

This group will be prescribed a dose of antibiotics (Septra 2mg/kg)

placebo comparator: Probiotic plus placebo

Receive probiotic plus an antibiotic placebo

active comparator: probiotics plus antibiotic

This group will be on a dose of probiotics (2 capsules; 5 billion total organisms of L. rhamnosus GR-1 and L. reuteri RC-14 per capsule) plus a antibiotic (Septra)

Interventions

Antibiotic

2 mg/kg per day via oral ingestion.

Probiotic

2 capsules; 5 billion total organisms of L. rhamnosus GR-1 and L. reuteri RC-14 per capsule

Primary outcome measure

  • Side effects [ Time Frame: Once a week for the duration of the study. The length of the study will be 6 months from the first baseline visit after the patient has been enrolled in the study and the first dispense of the study drug has been completed. ]

Central Contacts and Locations

Central contacts

Locations

London Health Sciences Centre

Recruiting

London, Ontario, Canada, N6A 4G5

Contacts

Principal Investigator:

Sumit Dave

More Information

Sponsor

London Health Sciences Centre

Last update posted

Sep 9, 2021

Last verified

Sep, 2021

Keywords

  • urinary tract infection
  • antibiotic prophylaxis
  • probiotics
  • neurogenic bladder
  • clean intermittent catheterization

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by London Health Sciences Centre on 2021-09-09.