Recurrent Urinary Tract Infections in Women

2

Review clinical trials related to Recurrent Urinary Tract Infections in Women. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Trial of D-mannose for the Prophylaxis of Recurrent Urinary Tract Infections

A randomized, double-blind, placebo-controlled, 12-month study to determine the effectiveness of D-mannose (2g daily) supplementation in rUTI (recurrent urinary tract infection) prevention in post-menopausal women.

Participants needed: 90
Trial details
Age: 55-85Biological sex: FemaleType: InterventionalSponsor: University of Texas Southwestern Medical CenterUpdated: Sep 22, 2025Locations: 1
Eligibility criteria

Female, post-menopausal, age ≥ 55 years old [+4]

Current use of D-mannose. Patients willing to stop taking D-mannose will be offe... [+23]

Status: Recruiting

Evaluate the Efficacy and Safety of U101 Oral Capsules in the Prevention of Uncomplicated rUTIs in Women

The goal of this clinical trial is to learn if drug U101 works to prevent recurrent urinary tract infection (rUTI) in women (≥ 20 and \< 76 years old) with a medical history. It will also investigate the safety and the impact on the Quality of Life improvement of drug U101. The main questions it aims to answer are: * Does the drug prevent or decrease the recurrence of urinary tract infection (UTI) during the 24-week treatment? * Will the Quality of Life be improved during the 24-week treatment? * What medical problems do participants have when taking drug U101? Researchers will compare drug U101 to a placebo (a look-alike substance that contains no drug) to see if drug U101 works to prevent rUTI. Participants will: * Orally take drug U101 or placebo every day for 24 weeks in the main study, three times per day (TID) for 8 weeks and twice per day (BID) for 16 weeks. * Visit the site once every 4 weeks for checkups and tests during the main study. * be asked to enroll in extensional study (the open-label extension (OLE) with drug U101 treatment or the Safety Follow-Up Visits with no investigational product treatment) for 24 weeks after they complete the 24-week main study. * Visit the site when the suspected UTI occurred during the main study or the extension study.

Participants needed: 348
Trial details
Phase: Phase 3Age: 20-75Biological sex: FemaleType: InterventionalSponsor: TCM Biotech International Corp.Updated: Sep 22, 2025Locations: 13
Eligibility criteria

Provide a signed informed consent form. [+4]

Females who are pregnant, nursing, have a desire for pregnancy or have a positiv... [+28]