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Oral Lactobacillus Supplementation as Treatment for Overactive Bladder Syndrome: A Randomised Controlled Trial

RecruitingNAAges 18 Years - anyFemaleMedical University of Vienna
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In plain words

What the trial is, and whether it could suit you

Background: Overactive bladder describes a syndrome characterized by frequent urges to urinate and increased urination with or without nocturia and with or without urinary incontinence. Overactive bladder affects approximately 13% of older women and thus represents a condition with high prevalence. Affected women report significant limitations in daily life, as well as social isolation. Despite the high occurrence of this condition, therapeutic options are limited, partly because the etiology of this condition is not fully understood. Increasingly, studies suggest an imbalance in the urogenital microbiome as a possible cause of the development of the condition. Therefore, the aim of this study is to test, whether the oral administration of a lactobacillus preparation can lead to a reduction in symptoms. Design: Randomized controlled study Methods: Intake of OMNi BiOTiC® 41167 or placeb

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📋 Eligibility rules (as published)
Inclusion Criteria: * diagnosis of overactive bladder syndrome or mixed urinary incontinence with predominance of overactive bladder symptoms Exclusion Criteria: * under age 18 * neurogenic overactive bladder
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What it tests

  • OMNi BiOTiC® 41167
  • Placebo
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Where

1 site
Medical University of Vienna
Vienna, Austria
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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