University of Texas Southwestern Medical Center
Dallas, Texas, 75390, United States
Location status: Recruiting
Location contact
Philippe E Zimmern, MD
PRINCIPAL_INVESTIGATOR
Sonobia Garrett, BSHS
CONTACT
CONTACT
NCT Number: NCT06940622
A randomized, double-blind, placebo-controlled, 12-month study to determine the effectiveness of D-mannose (2g daily) supplementation in rUTI (recurrent urinary tract infection) prevention in post-menopausal women.
Interested in participating?
Request Info55 year–85 year
Female
Interventional
Not applicable
Dallas, Texas, 75390, United States
Location status: Recruiting
Philippe E Zimmern, MD
PRINCIPAL_INVESTIGATOR
Sonobia Garrett, BSHS
CONTACT
CONTACT
The proposed study on D-mannose prophylaxis is designed to address a critical unmet medical need to improve the understanding and prevention of rUTI (recurrent urinary tract infection) in post-menopausal women, a population disproportionately affected by rUTI and understudied. The efficacy of D-mannose on preventing uncomplicated rUTI will be elucidated, and additional study measures (including urine culture and one-hour D-mannose test results) may help establish an ideal candidate for responding to daily D-mannose intake over time. The proposed study will follow CONSORT guidelines for randomized clinical trial studies.
Aim 1. Test the hypothesis that D-mannose provides effective rUTI prophylaxis in post-menopausal women over 6 months.
Aim 2. Test the hypothesis that D-mannose provides effective rUTI prophylaxis in post-menopausal women beyond 6 months and up to one year.
The overarching hypotheses are that (1) D-mannose will be found superior to placebo in preventing rUTI in post-menopausal women over 6 months as suggested by one prior RCT7 (Aim 1) and (2) D-mannose will remain effective for rUTI prophylaxis up to one year (Aim 2).
Ninety (90) women currently UTI-free and with a history of uncomplicated rUTI, defined as ≥ 2 symptomatic UTIs in 6 months or ≥ 3 symptomatic UTIs in 12 months, will be enrolled and randomized (2:1 ratio) to receive D-mannose (2g, i.e., 4 x 500mg capsules) or placebo daily for 12 months.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Box 1 Supplements to avoid
D-mannose (2g, i.e., 4 x 500mg capsules) daily for 12 months.
Placebo daily for 12 months.
Time frame: Through study completion, an average of 5 years
To determine whether prophylaxis with D-mannose reduces the incidence of UTI episodes compared to placebo. "Failure rate," defined as having 2 UTIs in 6 months or 3 in one year.
Time frame: Through study completion, an average of 5 years
To investigate if D-mannose reduces the need for antibiotic use due to recurrent UTIs (measured as number of antibiotic courses for symptomatic culture-proven UTI episodes) compared to placebo.
Number of UTI antibiotic treatments during the 6 months of treatment. If the participant receives >1 antibiotic course for UTI without symptom relief, it is regarded as one episode and counted as one antibiotic treatment. If there has been an asymptomatic period of at least 14 days in between two UTI antibiotic courses, this will be regarded as a new antibiotic treatment.
Time frame: Through study completion, an average of 5 years
To investigate if D-mannose reduces the severity of UTI symptoms compared to placebo. Record symptom severity using a validated UTI symptom assessment questionnaire.
Time frame: Through study completion, an average of 5 years
To determine the frequency of serious adverse events associated with D-mannose. Number of participants who experienced adverse events >= Grade 3, as defined by Common Terminology Criteria for Adverse Events by CTCA version 5.0.
Contact information is provided by the study sponsor or research team.
Jessica de Araujo Paula
CONTACT
Meghan Leak
CONTACT
University of Texas Southwestern Medical Center
Other
A Randomized Controlled Trial of D-mannose for the Prophylaxis of Recurrent Urinary Tract Infections in Post-menopausal Women
Acronym: DmannoseRCT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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