CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 84 enrolled
Drug / intervention
Bupivacaine +1 moredrug
Likely dose
Bupivacaine 20 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/NCT02660918
NCT02660918N/ACompleted
CompareCT.gov

Decreasing Postoperative Pain Following Endometrial Ablation: A Randomized Controlled Trial

Christiana Care Health Services·interventional·Posted Jan 21, 2016·Updated Aug 28, 2019

In Brief

A clinical study evaluating Bupivacaine and Normal Saline for Postoperative Pain. Completed, enrolled 84 participants across 1 site.

Detailed Summary

To determine whether paracervical injection of long acting local anesthesia decreases postoperative pain following endometrial ablation under general anesthesia.

Study Details

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

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedJan 21, 2016
Enrollment StartApr 1, 2016
Primary CompletionMar 1, 2017
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 10.4 years ago

Interventions

Bupivacainedrug

Paracervical injection of 20 mL 0.25% Bupivacaine at the completion of the procedure

Normal Salineother

Equal volume injection of normal saline with the same paracervical technique