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] — DRUGAll 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 antibioticAll patients will receive probiotics for this, only those with a UTI will get ciprofloxacin.
- No Intervention: ControlPatients will get standard of care treatment.
Primary Outcome Measure
Reduction in UTI episodes [ Time Frame: 6 months ]
Central Contacts
- Mehreen Arshad, MD3122274080
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Lurie Children's Hospital | Chicago | Illinois | 60611 |
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