An Efficacy Study of a Dietary Supplement Drink Mix for Urinary Health Improvement
ConditionUTI's
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-75
SponsorBonafide Health
About this trial
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.
Eligibility criteria
Qualifiers
Healthy biological females who are 18-75 years of age (inclusive).
Have a history of recurrent uncomplicated UTI (≥2 UTIs in the last 6 months and/or ≥3 UTIs in the last 12 months).
Are within 7 days of the enrollment trigger event (acute UTI).
In good general health (no active or uncontrolled diseases or conditions besides recurrent UTIs) and able to consume the study product.
Disqualifiers
Individuals who are lactating, pregnant, or planning to become pregnant during the study.
Active participation in a clinical trial.
Use of any treatment for menopausal outcomes or other concomitant treatments.
Have a known sensitivity, intolerability, or allergy to any of the study products or their excipients.
Trial design
Treatments tested in this trial
- FLUSH
Treatment groups
210 Participants
are divided into 3 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov