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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
AmPurity Nutraceuticals, LLC
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Recurrent Urinary Tract Infection focused on measuring uncomplicated recurrent urinary tract infection

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

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

    First Posted
    July 13, 2018
    Last Updated
    January 8, 2020
    Sponsor
    AmPurity Nutraceuticals, LLC
    Collaborators
    Arkansas Urology
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    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

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    Nutritional Supplementation for Recurrent Urinary Tract Infections in Women

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