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Bupivicaine to Reduce Postoperative Pain in Laparoscopic Ventral Hernia Repair

Postoperative Pain Clinical Trial

Official title:
Intraoperative Local Anesthesia for Management of Postoperative Pain Following Laparoscopic Ventral Hernia Repair: a Prospective Double-blind Randomized Trial

Clinical Trial Summary

The investigators are testing to see if infusion of bupivicaine between the mesh and abdominal wall can reduce postoperative pain and decrease use of narcotics in the postoperative setting.

Clinical Trial Description

The primary objective of this study is to test different methods for pain management following laparoscopic ventral hernia repair. We hypothesize that local analgesic injection between the abdominal wall and mesh intraoperatively during laparoscopic ventral hernia repair will result in a 20% decrease in the use of post-surgery pain medication in the first four hours after surgery. ;

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01530815
Study type Interventional
Source Chang, Steve S., M.D.
Contact Steve Chang, MD
Phone 805-637-0217
Email s1chang@sbch.org
Status Recruiting
Phase N/A
Start date August 2011
Completion date January 2013
View Details
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