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Decreasing Postoperative Pain Following Endometrial Ablation

NCT02660918 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 84

Last updated 2019-08-28

Study results available
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Summary

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

Conditions

  • Postoperative Pain

Interventions

DRUG

Bupivacaine

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

OTHER

Normal Saline

Equal volume injection of normal saline with the same paracervical technique

Sponsors & Collaborators

  • Christiana Care Health Services

    lead OTHER

Principal Investigators

  • Jordan Klebanoff, MD · Christiana Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
55 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-04-30
Primary Completion
2017-03-31
Completion
2017-03-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02660918 on ClinicalTrials.gov