Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07453693

An Efficacy Study of a Dietary Supplement Drink Mix for Urinary Health Improvement

A Randomized, Controlled Trial Evaluating the Efficacy of the FLUSH Dietary Supplement Drink Mix to Improve Urinary Health Measures

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
210 (estimated)
Sponsor
Bonafide Health · Industry
Sex
Female
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

This is a 6-month, three-arm randomized controlled trial evaluating the efficacy and safety of a dietary supplement drink mix on urinary health outcomes in adult females. Participants will be randomly assigned to one of three study arms and followed for six months to assess changes in urinary health measures.

Detailed description

Urinary tract infections (UTIs) are extremely common, affecting up to 60% of women in their lifetime, with 20-40% experiencing recurrent infections. Recurrent UTIs-defined as two infections in six months or three in one year-create a significant burden on quality of life and healthcare costs. Antibiotics are the standard treatment, but repeated use can contribute to antibiotic resistance, incomplete bacterial clearance, and disruption of the microbiome. Non-antibiotic approaches, such as D-mannose, vitamins, and hydration support, have shown potential to help reduce UTI recurrence. D-mannose may prevent E. coli-the most common UTI-causing bacteria-from adhering to the urinary tract, while vitamins and electrolytes may support hydration, urinary pH, and immune function. This clinical trial will evaluate the efficacy of a dietary supplement drink mix containing D-mannose, vitamins, and electrolytes in improving urinary health outcomes over a 6-month period in adult females. The goal is to determine whether this non-antibiotic approach can support urinary health and help reduce factors associated with recurrent UTIs.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTFLUSH2g D-Mannose drink mix

Timeline

Start date
2025-07-07
Primary completion
2026-12-15
Completion
2026-12-15
First posted
2026-03-06
Last updated
2026-03-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07453693. Inclusion in this directory is not an endorsement.