drugset / Trial / NCT06953271

Methenamine Hippurate Following Intradetrusor OnabotulinumtoxinA Injection

NCT06953271

Phase 4 Not yet recruiting 164 enrolled Women and Infants Hospital of Rhode Island
RandomizedParallel-groupOpen-labelPrevention

Summary

The goal of this clinical trial is to compare methenamine hippurate prophylaxis to routine antibiotic prophylaxis following onabotulinumtoxinA (BOTOX-A) injections in women with overactive bladder (OAB). Participants will be randomly selected to receive one of the two post-procedural prophylaxis medications. The primary outcome measure will be urinary tract infection (UTI) rates within 30 days from the BOTOX-A procedure. Secondary outcomes will assess patient satisfaction with the two post-procedural prophylaxis medications.

Timeline

Start
2025-05-15
Primary completion
2026-05-01
Completion
2027-01-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Methenamine Hippurate Unknown 1 g Oral
Comparator Nitrofurantoin Unknown Oral
Comparator amoxicillin/clavulanic acid Unknown Oral
Comparator trimethoprim/sulfamethoxazole Unknown Oral