CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 132 enrolled
Drug / intervention
Bupivacaine +1 moredrug
Likely dose
Bupivacaine 10 mlfrom 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/NCT01534416
NCT01534416N/ACompleted

Use of Paracervical Block in Laparoscopic Gynecologic Surgery: A Randomized Controlled Trial

Icahn School of Medicine at Mount Sinai·interventional·Posted Feb 16, 2012·Updated Dec 20, 2017

In Brief

A clinical study evaluating Bupivacaine and Normal Saline for Postoperative Pain and 2 related conditions. Completed, enrolled 132 participants across 1 site.

Detailed Summary

The purpose of this study is to determine the effectiveness of placing numbing medication around the cervix prior to performing laparoscopic gynecologic surgery in decreasing pain after surgery. The study focuses on laparoscopic hysterectomies and robotic-assisted myomectomies. It will assess whether patients who receive the medication experience less pain and require less pain medication post operatively and if it helps reduce the number of patients who require hospitalization for pain control following surgery.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedFeb 16, 2012
Enrollment StartSep 1, 2011
Primary CompletionSep 1, 2013
TodayJul 2, 2026
Enrollment to primary: 2 yearsPosted 14.4 years ago

Interventions

Bupivacainedrug

Subjects are injected paracervically with 10 ml of 0.5% bupivacaine with 1:200000 units epinephrine prior to surgical incision.

Normal Salinedrug

Subjects are injected paracervically with 10 ml of normal saline prior to surgical incision.