Changes in the Urinary Microbiome and Metabolome During Treatment of the Overactive Bladder in Female Patients

May 1, 2025 updated by: University Hospital Ostrava
This is a non-interventional study that will not pose any burden for the participants. The study subjects will be examined and treated in a standard manner according to current clinical recommendations for the treatment of overactive bladder (OAB). A portion of urine samples, which are routinely collected for biochemical and culture examinations as part of the diagnostic process, will be sent for examination of the characteristics of the urinary microbiome and metabolome (UMM) before and after treatment.

Study Overview

Detailed Description

Participation in the study will be offered to female patients who seek treatment for OAB symptoms themselves or are referred to centers participating in the project if a clinical diagnosis of idiopathic OAB is established in their case as part of the standard examination process.

Patients will be approached by one of the authorized team members with information about the possibility of participating in this study. If the patient is interested in participating in the study, she will give written informed consent to participate in the study. Subsequently, the inclusion and exclusion criteria for participation in the study will be verified and a standardized urine collection will be performed to examine the characteristics of UMM. At the same time, the patient will fill in standard questionnaires used to determine the severity of OAB symptoms.

To research changes in UMM during OAB treatment, patients will be divided into a group with a good treatment response (responders) and a group without a good treatment response (non-responders). The primary indicator of a good treatment effect (definition of responder) is a reduction in the number of episodes of severe urgency with or without urge incontinence over 3 days documented by a voiding diary by more than 50% compared to the state before treatment. Based on the available data, treatment success is anticipated in 60% of patients.

Subsequently, the study participants will be treated with standard drug treatment for five weeks. They will then be invited to evaluate the effect of treatment using standard symptom questionnaires. At the same time, a control standardized urine collection will be performed to examine the characteristics of UMM. The patients will then end their participation in the study and will continue their treatment according to the valid clinical recommendations for treatment.

Study Type

Observational

Enrollment (Estimated)

80

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Praha, Czechia, 14059
        • Recruiting
        • Thomayer University Hospital
        • Contact:
        • Principal Investigator:
          • Roman Zachoval, prof., MD, PhD
      • Praha, Czechia, 14200
        • Recruiting
        • Institute of Microbiology of the Czech Academy of Sciences
        • Contact:
        • Principal Investigator:
          • Andrea Palyzová, RNDr., PhD
      • Praha, Czechia, 18081
        • Recruiting
        • University Hospital Bulovka
        • Contact:
        • Principal Investigator:
          • Jan Hrbáček, MD, PhD
        • Sub-Investigator:
          • Petr Hubka, Assoc. Prof., MD, PhD
    • Moravian-Silesian Region
      • Ostrava, Moravian-Silesian Region, Czechia, 70852
        • Recruiting
        • University Hospital Ostrava
        • Contact:
        • Principal Investigator:
          • Jan Krhut, prof., MD, PhD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Adult women with symptoms of overactive bladder persisting longer than three months willing to participate in the study.

Description

Inclusion Criteria:

  • Adult women over 18 years of age
  • Written consent to participate in the study
  • Willingness to undergo OAB evaluation and treatment according to the protocol
  • OAB symptoms lasting longer than 3 months
  • At least 3 episodes of severe urgency with or without urge incontinence within 3 days documented by voiding diary
  • OAB symptom score V8 questionnaire ≥ 8

Exclusion Criteria:

  • Known congenital developmental defects of the urinary tract (congenital hydronephrosis, vesicoureteral reflux, renal agenesis and hypoplasia, multicystic and polycystic kidneys)
  • Any previous treatment for OAB
  • Recurrent urinary tract infections (more than 3 episodes in the last 12 months)
  • Presence of a foreign body in the urinary tract - urolithiasis, urinary catheter, ureteral stent
  • Acute or chronic diseases with possible influence on the function of the lower urinary tract (LUT)
  • Rheumatoid arthritis
  • Diabetes mellitus

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Overactive Bladder Patients
Patients with the symptoms of overactive bladder will be enrolled in this study group
Microbiological and metabolomic analysis of a urine sample will be performed in the study subjects, before and after the end of the treatment.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Proportion of responders to the OAB treatment
Time Frame: 6 weeks
The proportion of study subjects responding to the treatment of OAB symptoms will be observed.
6 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in UMM characteristics between both groups
Time Frame: 6 weeks
Changes in UMM characteristics based on laboratory examination will be compared between the two study groups (responders vs non-responders)
6 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jan Krhut, prof., MD, PhD, University Hospital Ostrava

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

May 1, 2025

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2027

Study Registration Dates

First Submitted

April 3, 2025

First Submitted That Met QC Criteria

April 3, 2025

First Posted (Actual)

April 10, 2025

Study Record Updates

Last Update Posted (Actual)

May 4, 2025

Last Update Submitted That Met QC Criteria

May 1, 2025

Last Verified

May 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

There is no plan to make individual participant data available to other researchers. The data may be provided upon request.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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