Effects of Microbiological and Immunological Factors on the Lower Urinary Tract

NCT07494864 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 800

Last updated 2026-03-27

No results posted yet for this study

Summary

Millions of patients of all ages suffer worldwide from diverse urinary pathologies, such as lower urinary tract (LUT) dysfunction, bladder pain syndrome, urinary tract infections (UTIs), or bladder cancer. The research project investigates the interplay between the bladder and the microbiome. The goal is to evaluate the association of microbiological and immunological factors with lower urinary tract health in humans.

Conditions

  • Asymptomatic Bacteriuria in Subjects Not Requiring Assisted Bladder Emptying
  • Asymptomatic Bacteriuria in Subjects Relying on Some Type of Catheter
  • Recurrent Non-catheter Associated UTIs
  • Acute Catheter-associated UTI (CAUTI)
  • Recurrent Catheter-associated UTI (CAUTI)
  • Chronic Pelvic Pain
  • Non-neurogenic Overactive Bladder Syndrome / LUT Symptoms
  • Non-muscle-invasive Bladder Cancer

Sponsors & Collaborators

  • Kessler Group

    collaborator UNKNOWN
  • Rätsch Group

    collaborator UNKNOWN
  • Slack Group

    collaborator UNKNOWN
  • Boyman Group

    collaborator UNKNOWN
  • Sunagawa Group

    collaborator UNKNOWN
  • Zamboni Group

    collaborator UNKNOWN
  • Loessner Group

    collaborator UNKNOWN
  • McKinney Group

    collaborator UNKNOWN
  • Nexus

    collaborator UNKNOWN
  • Research Group Dirk Bumann

    collaborator UNKNOWN
  • Research Group Christoph Dehio

    collaborator UNKNOWN
  • University of Zurich

    lead OTHER

Principal Investigators

  • Thomas Kessler, Prof. Dr. med. · Universitätsklinik Balgrist

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-06-01
Primary Completion
2026-11-30
Completion
2026-11-30

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07494864 on ClinicalTrials.gov