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Clinical Trials/NCT01530815
NCT01530815
Unknown
Not Applicable

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

Chang, Steve S., M.D.1 site in 1 country80 target enrollmentAugust 2011

Overview

Phase
Not Applicable
Intervention
Bupivicaine Infusion
Conditions
Postoperative Pain
Sponsor
Chang, Steve S., M.D.
Enrollment
80
Locations
1
Primary Endpoint
Pain
Last Updated
14 years ago

Overview

Brief 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.

Detailed 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.

Registry
clinicaltrials.gov
Start Date
August 2011
End Date
January 2013
Last Updated
14 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Chang, Steve S., M.D.
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patient must be scheduled for a laparoscopic ventral hernia repair at SBCH. If any additional procedure is performed, the subject will be excluded from the study
  • Age 18 or older
  • Patient must agree to complete pain journal postoperatively
  • Informed consent signed and dated by patient. Consenting through a legally authorized guardian will not be accepted due to the necessity of completing a subjective pain journal

Exclusion Criteria

  • Any surgical procedure occurring besides the study procedure
  • Any allergy or sensitivity to bupivicaine or its derivatives
  • Less than 18 years of age
  • Patient unable to self report in pain journal due to cognitive disabilities
  • Discharged less than 4 hours post-surgery

Arms & Interventions

Bupivicaine Infusion

We will infuse bupivicaine between the abdominal wall and mesh to try and reduce postoperative pain

Intervention: Bupivicaine Infusion

Outcomes

Primary Outcomes

Pain

Time Frame: 24 hours

We will measure pain based on pain journal and usage of postoperative pain medication

Study Sites (1)

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