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Experimental: Limosilactobacillus Supplement for Urinary Tract Infection
Study Summary
This trial will see if Limosilactobacillus reuteri 3613 can prevent or reduce UTIs in women w/ a history of recurrent UTIs vs. a placebo.
- Urinary Tract Infection
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
Frequently Asked Questions
Is recruitment still open for this experimental research project?
"According to the source material on clinicaltrials.gov, this experiment is still recruiting members and was first established on May 7th 2021. The information was recently updated on March 20th of this year."
Would individuals who are younger than 75 years old be considered acceptable candidates for this experiment?
"Per the specified inclusion criteria, individuals between 18 and 65 are eligible for this clinical trial. However, 358 studies cater to minors while 1492 trials target elderly patients."
Who has access to the opportunity of joining this medical experiment?
"Prospective participants should meet the age requirements of 18-65 and display symptoms of urinary tract infection to be eligible for this trial. This research is recruiting a total of 130 individuals."
What is the primary intent behind this clinical investigation?
"The primary measure of efficacy over a 6-month period will be the proportion of participants who experience at least one symptomatic urinary tract infection (UTI). Additionally, secondary outcomes include the proportions and total number of UTIs experienced across product groups from V2 to Final V5, as well as any differences between probiotic treatment and placebo in terms of time for first UTI occurrence within this same timeframe."
How many participants have been enlisted for this clinical investigation?
"Yes, according to the information provided by clinicaltrials.gov, this medical trial is still recruiting patients. It was initially posted on May 7th 2021 and updated most recently on March 20th 2023, with a target of 130 participants from one site."
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