Urinary Tract Infections Clinical Trial
— NO-UTIOfficial title:
The Efficacy and Cost-effectiveness of a 24-hour Course of metheNamine Hippurate for Preventing Post-Operative Urinary Tract Infection
NCT number | NCT02358993 |
Other study ID # | 820117 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | December 2014 |
Est. completion date | September 30, 2020 |
Verified date | February 2022 |
Source | University of Pennsylvania |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The investigators will determine the efficacy of an innovative short regimen of methenamine hippurate on prevention of post-operative UTI in patients requiring short-term catheterization after pelvic reconstructive surgery through a single-blind, randomized controlled trial. Primary outcome will be the rate of symptomatic UTI within 3 weeks of catheter removal. The investigators will study cost-effectiveness, antibiotic resistance profiles, and adverse drug effects. Findings may reduce antibiotic use and nosocomial UTIs.
Status | Completed |
Enrollment | 201 |
Est. completion date | September 30, 2020 |
Est. primary completion date | September 30, 2020 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - female; - patients who are able to read and write English; - 18 years of age or older; - underwent surgery for pelvic organ prolapse, urinary incontinence, or both; - require post-operative short-term transurethral catheterization for greater than 24 hours. Exclusion Criteria: - patients undergoing surgical intervention for sacral neuromodulation, or mesh excision; - patients requiring long-term catheterization secondary to injury to the urinary tract; - patients who pass their post-operative trial void and thus, do not require additional catheterization; - patients requiring catheterization for less than 24 hours; - pregnant patients; - patients who are breast-feeding; - allergy to methenamine hippurate or fluroquinolones (either ciprofloxacin or levofloxacin); - impaired renal or hepatic function; - pre-operative urinary retention; - patients who are currently using sulfonamides; - patients who have severe dehydration; - patients using tizanidine; - patients sensitive to quinolones class; - patients using theophylline; patients with myasthenia gravis; - patients with prolongation of QT interval. |
Country | Name | City | State |
---|---|---|---|
United States | Chestnut Hill Hospital | Philadelphia | Pennsylvania |
United States | Hospital of the University of Pennsylvania | Philadelphia | Pennsylvania |
United States | Penn Presbyterian Medical Center | Philadelphia | Pennsylvania |
United States | Pennsylvania Hospital | Philadelphia | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
University of Pennsylvania |
United States,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Rate of UTI Consistent With NHSN Criteria | We plan to analyze the prevalence of UTI in this population that meet the definitions of symptomatic UTI and catheter-associated UTI according to the National Healthcare Safety Network criteria. | 3 weeks post-operative | |
Primary | Treatment of Clinically Suspected UTI - Using Intent to Treat Analysis | This is defined as any symptomatic UTI requiring treatment with antibiotics as determined by the development of 2 or more of the following symptoms, in the absence of vaginal symptoms: urinary frequency; urinary urgency; dysuria; fever over 38oC/100.4oF; suprapubic, flank, or back pain; and/or chills. | 3 weeks post-operative | |
Primary | Treatment of Clinically Suspected UTI - Per Protocol | This is defined as any symptomatic UTI requiring treatment with antibiotics as determined by the development of 2 or more of the following symptoms, in the absence of vaginal symptoms: urinary frequency; urinary urgency; dysuria; fever over 38oC/100.4oF; suprapubic, flank, or back pain; and/or chills. | 3 weeks post-operative | |
Secondary | Number of Participants With Culture-positive Symptomatic UTI | All patients will be encouraged to submit urine cultures prior to treatment, but this is not always possible. Amongst patients who undergo urine culture as part of standard of care for UTI, the rate of positive cultures will be identified. | 3 weeks post-operative | |
Secondary | Antibiotic Resistance of Culture-positive Symptomatic UTI | All patients who submit urine cultures that are positive will have sensitivities performed as per standard care. The prevalence of bacterial species and sensitivities will be collected | 3 weeks post-operative | |
Secondary | Cost-effectiveness of Prophylaxis With Methenamine Hippurate for Prevention of Post-operative UTI Compared to Prophylaxis With Fluoroquinolones | Routine costs of prevention of UTI with methenamine hippurate prophylaxis will be compared with costs of prevention of UTI with fluoroquinolone prophylaxis. We plan to capture costs for each direct medical service use, direct non-medical items, and indirect items related to post-operative UTIs in each arm of the trial. | 3 weeks post-operative | |
Secondary | Prevalence of Side Effects | Adverse effects from the administration of methenamine and fluoroquinolones will be collected. | within 24 hours of administration |
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