RECRUITINGINTERVENTIONAL
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
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.
Who May Be Eligible (Plain English)
Who May Qualify:
1. Healthy biological females who are 18-75 years of age (inclusive).
2. Have a history of recurrent uncomplicated UTI (≥2 UTIs in the last 6 months and/or ≥3 UTIs in the last 12 months).
3. Are within 7 days of the enrollment trigger event (acute UTI).
4. In good general health (no active or uncontrolled diseases or conditions besides recurrent UTIs) and able to consume the study product.
5. BMI 18.5-39.9 kg/m\^2
6. Have reliable, stable access to Wi-Fi and a smart phone/device.
7. Willing and able to agree to the requirements and restrictions of this study, willing to give voluntary consent, able to understand and read questionnaires, and able to carry out all study-related procedures.
Who Should NOT Join This Trial:
1. Individuals who are lactating, pregnant, or planning to become pregnant during the study.
2. Active participation in a clinical trial.
3. Use of any treatment for menopausal outcomes or other concomitant treatments.
4. Have a known sensitivity, intolerability, or allergy to any of the study products or their excipients.
5. History of hyperkalemia (high potassium).
6. History of Chronic Kidney Disease.
7. Introduction of antibiotics unrelated to a UTI occurrence during the trial period.
8. Current use of D-mannose (participants may complete a 2-week waiting period after previous treatment).
9. Has previously used the FLUSH product.
10. Current use of antibiotic-based prophylaxis.
11. History of Diabetes mellitus (Type 1 and/or 2).
12. Use of vaginal and/or local estrogen therapy (permitted if stable dose longer than 90 days).
13. Active or suspected vaginitis.
14. Started a new nonantibiotic-based prophylaxis within the last 90 days.
15. Use of probiotics (permitted if orally administered with stable dose longer than 90 days).
16. Use of indwelling or intermittent urinary catheterization.
17. Diagnosis of overactive bladder (OAB) or interstitial cystitis /bladder pain syndrome (IC/BPS).
...See full criteria on ClinicalTrials.gov
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
1. Healthy biological females who are 18-75 years of age (inclusive).
2. Have a history of recurrent uncomplicated UTI (≥2 UTIs in the last 6 months and/or ≥3 UTIs in the last 12 months).
3. Are within 7 days of the enrollment trigger event (acute UTI).
4. In good general health (no active or uncontrolled diseases or conditions besides recurrent UTIs) and able to consume the study product.
5. BMI 18.5-39.9 kg/m\^2
6. Have reliable, stable access to Wi-Fi and a smart phone/device.
7. Willing and able to agree to the requirements and restrictions of this study, willing to give voluntary consent, able to understand and read questionnaires, and able to carry out all study-related procedures.
Exclusion Criteria:
1. Individuals who are lactating, pregnant, or planning to become pregnant during the study.
2. Active participation in a clinical trial.
3. Use of any treatment for menopausal outcomes or other concomitant treatments.
4. Have a known sensitivity, intolerability, or allergy to any of the study products or their excipients.
5. History of hyperkalemia (high potassium).
6. History of Chronic Kidney Disease.
7. Introduction of antibiotics unrelated to a UTI occurrence during the trial period.
8. Current use of D-mannose (participants may complete a 2-week washout period).
9. Has previously used the FLUSH product.
10. Current use of antibiotic-based prophylaxis.
11. History of Diabetes mellitus (Type 1 and/or 2).
12. Use of vaginal and/or local estrogen therapy (permitted if stable dose longer than 90 days).
13. Active or suspected vaginitis.
14. Started a new nonantibiotic-based prophylaxis within the last 90 days.
15. Use of probiotics (permitted if orally administered with stable dose longer than 90 days).
16. Use of indwelling or intermittent urinary catheterization.
17. Diagnosis of overactive bladder (OAB) or interstitial cystitis /bladder pain syndrome (IC/BPS).
18. Urologic procedure within 6 months prior to trial enrollment.
19. History of structural urinary tract disease.
20. History of Lichen sclerosis.
21. Use of potassium-sparing medications. o E.g., Spironolactone (used for PCOS) (potassium-sparing diuretic); ACE inhibitors and ARBs; systemic calcineurin inhibitors.
Treatments Being Tested
DIETARY_SUPPLEMENT
FLUSH
2g D-Mannose drink mix
Locations (1)
Bonafide Health
Harrison, New York, United States