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Transverse Abdominal Plane Anesthesia for Abdominal Wall Reconstruction

NCT02274077 · Status: WITHDRAWN · Phase: PHASE4 · Type: INTERVENTIONAL

Last updated 2016-07-11

No results posted yet for this study

Summary

The aim of this study is to evaluate the short-term postoperative outcomes in the abdominal wall reconstruction population using an intraoperative local anesthetic infusion. A prospective randomized double blind study of patients undergoing component separation will be performed in order to assess the following outcomes:

1. Length of Stay (LOS)
2. Return of bowel function
3. Narcotic pain medication requirements
4. Nausea and emesis
5. Pain scores

Conditions

  • Hernia, Ventral

Interventions

DRUG

EXPAREL

DRUG

Normal Saline

Sponsors & Collaborators

  • Chester Mays

    lead OTHER

Principal Investigators

  • Howard N Langstein, MD · University of Rochester Division of Plastic and Reconstructive Surgery

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-01-31
Primary Completion
2017-03-31
Completion
2017-06-30

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 NCT02274077 on ClinicalTrials.gov