drugset / Trial / NCT04807920

BOTOX® at the Time of Prolapse Surgery for OAB

NCT04807920 ↗

Phase 4 Unknown 138 enrolled Walter Reed National Military Medical Center
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of the study will be to assess the efficacy and safety of bladder BOTOX® for overactive bladder symptoms, such as urinary urgency and frequency, given at the time of prolapse surgery.

Timeline

Start
2021-09-23
Primary completion
2023-06
Completion
2023-06

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Botulinum toxin type A Protein / enzyme biologic 100 iu Other