CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 90 enrolled
Drug / intervention
Bupivacaine +2 moredrug
Likely dose
Bupivacaine 10mlfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01583166
NCT01583166N/ACompleted
CompareCT.gov

Voiding Function After Mid-Urethral Slings With and Without Local Anesthetic: Randomized Controlled Trial

University of Massachusetts, Worcester·interventional·Posted Apr 23, 2012·Updated Nov 28, 2018

In Brief

A clinical study evaluating Bupivacaine, Saline, and 1 other intervention for Stress Urinary Incontinence. Completed, enrolled 90 participants across 1 site.

Detailed Summary

The purpose of this study is to determine if there is a difference in post-operative voiding function between subjects receiving local anesthetic and those receiving placebo at the time of mid-urethral sling placement. The secondary objective is to evaluate pain after the procedure in the two groups.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsStress Urinary Incontinence
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedApr 23, 2012
Enrollment StartMar 1, 2012
Primary CompletionMay 1, 2016
TodayJul 2, 2026
Enrollment to primary: 4.2 yearsPosted 14.2 years ago

Interventions

Bupivacainedrug

10ml 0.5% bupivacaine

Salinedrug

10ml 0.9% sodium chloride

Epinephrinedrug

1:200,000 epinephrine