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

Part of paid clinical trials in Harrison, New York.

Sponsor
Bonafide Health
Study ID
NCT07453693
Status
Recruiting

Conditions

  • UTI's

Eligibility Criteria

Sex
FEMALE
Age
18 Years - 75 Years
Healthy Volunteers
Accepted

Interventions

  • FLUSH — DIETARY_SUPPLEMENT
    2g D-Mannose drink mix

Study Details

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.

Key Dates

Start date
Jul 7, 2025
Status verified
Mar 2026
Primary completion
Dec 15, 2026
Completion
Dec 15, 2026

Study Design

Enrollment
210 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION

Arms

  • Active Comparator: FLUSH Daily Dosing
    Daily dosing of FLUSH
  • Active Comparator: FLUSH 3-Day Dosing
    Dosing FLUSH once every 3 days and after sex if sexually active
  • No Intervention: Standard of Care
    No study product administered. Maintain current UTI prevention measures.

Primary Outcome Measure

Time to recurrence of clinically suspected UTI [ Time Frame: 6 months ]

Locations (1)

FacilityCityStateZIPSite coordinators
Bonafide HealthHarrisonNew York10528
Trisha VanDusseldorp, Senior Director of Clinical Research, PhD
233-266-2343
Trisha VanDusseldorp, PhD (PRINCIPAL_INVESTIGATOR)

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