A Novel Probiotic-antibiotic Combination to Prevent Recurrent Urinary Tract Infections

Part of paid clinical trials in Chicago, Illinois.

Sponsor
Ann & Robert H Lurie Children's Hospital of Chicago
Study ID
NCT06149676
Phase
EARLY_PHASE1
Status
Recruiting

Conditions

  • Recurrent Uti

Eligibility Criteria

Sex
ALL
Age
2 Years - 17 Years
Healthy Volunteers
Accepted

Interventions

  • Saccharomyces Boulardii 250 MG [Florastor] — DRUG
    All patients will get the probiotic to be taken daily. If UTI occurs with a sensitive pathogen, we will treat with ciprofloxacin

Study Details

Patients with recurrent UTI were randomized to receive either the probiotic Sacchromyces Boulardii at enrollment, and the intracellularly active Ciprofloxacin with their first UTI episode after enrollment, or they received standard of care treatment.

Key Dates

Start date
Feb 2, 2022
Status verified
Jan 2025
Primary completion
Dec 31, 2024
Completion
Dec 31, 2025

Study Design

Enrollment
35 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION

Arms

  • Experimental: Probiotic with or without antibiotic
    All patients will receive probiotics for this, only those with a UTI will get ciprofloxacin.
  • No Intervention: Control
    Patients will get standard of care treatment.

Primary Outcome Measure

Reduction in UTI episodes [ Time Frame: 6 months ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Lurie Children's HospitalChicagoIllinois60611
Mehreen Arshad
312-227-4080

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