Nutritional Supplementation for Recurrent Urinary Tract Infections in Women
Primary Purpose
Recurrent Urinary Tract Infection
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
WelTract
Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Recurrent Urinary Tract Infection focused on measuring uncomplicated recurrent urinary tract infection
Eligibility Criteria
Inclusion Criteria:
- Presenting with symptoms of UTI
- Presentation of 3rd or 4th simple cystitis of lower tract in the past 12 months
- Active infection at enrollment, confirmed and documented in medical record
- Cognitive capacity to consent and ability to undergo the consent process in English
Exclusion Criteria:
- Known allergy or intolerance to supplement ingredients
- Pregnant or planning to become pregnant or lactating
- Unwilling to commit to birth control use
- Use of related nutritional supplements
- Unwilling to halt berry extracts, polyphenols, antioxidants, d-mannose, vitamins
- Taken WelTract in past six months
- Unwilling to avoid probiotics, yogurt, apple or cranberry juice, hibiscus tea
- Certain comorbid or physical conditions
- History of febrile UTI
- Bladder catheter or urethral stents
- Use of topical hormones in urogenital areas
- Diabetes (i.e. taking diabetic medications) or glycosuria
- Intestinal diseases with malabsorption (e.g. Crohn's and celiac diseases)
- Severe renal impairment or kidney stones
- Neural problems (spinal cord injury or Multiple Sclerosis)
- Immunocompromised individuals
- Rheumatoid arthritis
- Lupus
- HIV
- Taking steroids or immunobiologic medications
- Prophylactic antibiotic use (e.g. post-coital)
- Other physician judgement
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Treatment
Control
Arm Description
WelTract
Inert Placebo
Outcomes
Primary Outcome Measures
UTI Recurrence
Time to recurrence of next UTI
Secondary Outcome Measures
Full Information
NCT ID
NCT03597152
First Posted
July 13, 2018
Last Updated
January 8, 2020
Sponsor
AmPurity Nutraceuticals, LLC
Collaborators
Arkansas Urology
1. Study Identification
Unique Protocol Identification Number
NCT03597152
Brief Title
Nutritional Supplementation for Recurrent Urinary Tract Infections in Women
Official Title
Nutritional Supplementation for Extending Time Between Recurrent Urinary Tract Infections in Women: a Randomized Double Blind Cross-over Trial
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Unknown status
Study Start Date
August 1, 2020 (Anticipated)
Primary Completion Date
January 14, 2022 (Anticipated)
Study Completion Date
December 31, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AmPurity Nutraceuticals, LLC
Collaborators
Arkansas Urology
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The study will test the ability of specially formulated nutritional supplement capsules to extend the time between recurrent urinary tract infections in women. This objective will be completed by enrolling women who have suffered from 3-4 uncomplicated UTIs in the past 12 months into a double blind placebo controlled cross-over trial. Cross-over and study completion are triggered by the next two UTI recurrences. The goal of the study is for the supplement to extend the time to the next UTI for study participants as compared to placebo.
Detailed Description
Background: Recurrent urinary tract infections (UTIs), i.e. having three or more infections in 12 months, present a common and serious health problem for women. Long-term prophylactic antibiotic use is one treatment approach though there are currently no consensus treatment strategies for chronic recurrent UTIs which makes development of antibiotic resistant bacterial strains a major concern. Alternatively, nutritional supplements such as those based on cranberry and the sugar d-mannose, have shown some mixed success as a complementary treatment for UTIs. Thus, identification of a multi-ingredient nutritional supplement which could reduce the recurrence of UTIs when applied in conjunction with standard of care would be valuable to the heath and healthcare of women.
Objective: The study will test the efficacy of a twice-daily nutritional supplement for extending the time between recurrent UTIs in women. The supplement is a commercially available product (WelTract, AmPurity LLC) whose capsules contain extracts from Hibiscus flowers and cranberry fruit, lactoferrin, D-mannose, and vitamins C and D.
Methods: The study design will be a randomized double-blind placebo-controlled cross-over trial. The primary outcome will be time to recurrence of next UTI. Women (age 18-75 yrs) will be enrolled at a private urology clinic upon presentation of their 3rd or 4th simple cystitis of the lower urinary tract in the past 12 months. Randomization and product consumption will occur concurrently with standard of care treatment (acute antibiotics) of the infection. Resolution of the infection will be confirmed by urine culture and supplement or placebo consumption will continue until UTI recurrence which will trigger cross-over. Again, standard of care will ensue and consumption of the supplement or placebo will continue until UTI recurrence which triggers participant study completion. Cross-over is not forced and the maximum allowable time to cross-over and/or complete the study is one year per participant. Side-effects will be monitored and reported.
Analysis Plan: The study plans to enroll a maximum of 250 women, intending to ensure that 150 women complete the study. Statistical analysis will be performed using both the non-parametric Log Rank test and the Gail and Simon method, each with different primary outputs (statistical significance and effect size, respectively). Both of these methods are suitable for comparing paired time-to-event measures as found in a cross-over design. The baseline sample size (N=150) was calculated using the Cox Proportional Hazard method, at 85% desired power, an alpha level 0.05, a representative hazard ratio of 0.7 from prior cranberry treatment trials, and allowing for up to 40% of the subjects to not complete the study due to reasons such as withdrawal or dropout.
Clinical Significance: The daily consumption of a scientifically-based multi-ingredient nutritional supplement may provide a safe and practical means to extend the time until recurrence of the next UTI for women who have suffered 3-4 UTIs in the past 12 months when applied in combination with standard of care.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Recurrent Urinary Tract Infection
Keywords
uncomplicated recurrent urinary tract infection
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
250 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Treatment
Arm Type
Experimental
Arm Description
WelTract
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Inert Placebo
Intervention Type
Dietary Supplement
Intervention Name(s)
WelTract
Intervention Description
Supplement commercially available from the sponsor containing powdered extracts from Hibiscus flowers and cranberry fruit, lactoferrin, D-mannose, and vitamins C and D
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Inert placebo custom manufactured for the sponsor
Primary Outcome Measure Information:
Title
UTI Recurrence
Description
Time to recurrence of next UTI
Time Frame
Variable for each participant over course of up to one year
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
Not based on self-representation
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Presenting with symptoms of UTI
Presentation of 3rd or 4th simple cystitis of lower tract in the past 12 months
Active infection at enrollment, confirmed and documented in medical record
Cognitive capacity to consent and ability to undergo the consent process in English
Exclusion Criteria:
Known allergy or intolerance to supplement ingredients
Pregnant or planning to become pregnant or lactating
Unwilling to commit to birth control use
Use of related nutritional supplements
Unwilling to halt berry extracts, polyphenols, antioxidants, d-mannose, vitamins
Taken WelTract in past six months
Unwilling to avoid probiotics, yogurt, apple or cranberry juice, hibiscus tea
Certain comorbid or physical conditions
History of febrile UTI
Bladder catheter or urethral stents
Use of topical hormones in urogenital areas
Diabetes (i.e. taking diabetic medications) or glycosuria
Intestinal diseases with malabsorption (e.g. Crohn's and celiac diseases)
Severe renal impairment or kidney stones
Neural problems (spinal cord injury or Multiple Sclerosis)
Immunocompromised individuals
Rheumatoid arthritis
Lupus
HIV
Taking steroids or immunobiologic medications
Prophylactic antibiotic use (e.g. post-coital)
Other physician judgement
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Katie O'Brien
Phone
501-219-8900
Ext
2002
Email
katie@arkansasurology.com
First Name & Middle Initial & Last Name or Official Title & Degree
Richard Dennis, PhD
Phone
501-960-8024
Email
protocols@att.net
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Richard D'Anna, MD
Organizational Affiliation
Arkansas Urology, Staff Physician
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
36041061
Citation
Cooper TE, Teng C, Howell M, Teixeira-Pinto A, Jaure A, Wong G. D-mannose for preventing and treating urinary tract infections. Cochrane Database Syst Rev. 2022 Aug 30;8(8):CD013608. doi: 10.1002/14651858.CD013608.pub2.
Results Reference
derived
Learn more about this trial
Nutritional Supplementation for Recurrent Urinary Tract Infections in Women
We'll reach out to this number within 24 hrs