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Clinical Trial Summary

The goal of this clinical trial is to evaluate if prophylactic antibiotics in urethral bulking are effective in reducing postprocedural urinary tract infections.


Clinical Trial Description

Urethral bulking is a minimally invasive surgical treatment option for stress urinary incontinence (SUI). One commonly reported post-procedural complication is urinary tract infection (UTI). UTI rates are variable where studies have reported rates from as low as 0% to as high as 40%. Along with this variability, the instructional inserts for various bulking agents have inconsistent recommendations for use of prophylactic antibiotics. The American Urologic Association recommends antimicrobial prophylaxis for cystourethroscopy procedures involving minor manipulation. Currently, there are no clear guidelines regarding the utility of prophylactic antibiotics for urethral bulking. The objective of our study is to determine the effectiveness of prophylactic antibiotics in urethral bulking for reducing post procedural UTIs. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06261736
Study type Interventional
Source Atlantic Health System
Contact Tess Gao, MD
Phone 973-971-7267
Email tess.gao@atlantichealth.org
Status Recruiting
Phase N/A
Start date October 24, 2023
Completion date May 2025

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