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_SUPPLEMENT2g 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 DosingDaily dosing of FLUSH
- Active Comparator: FLUSH 3-Day DosingDosing FLUSH once every 3 days and after sex if sexually active
- No Intervention: Standard of CareNo study product administered. Maintain current UTI prevention measures.
Primary Outcome Measure
Time to recurrence of clinically suspected UTI [ Time Frame: 6 months ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Bonafide Health | Harrison | New York | 10528 | Trisha VanDusseldorp, PhD (PRINCIPAL_INVESTIGATOR) |
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