Status:

COMPLETED

Study of the Effect of the Drug Gabapentin on Postoperative Pain and Incidence of Postoperative Nausea and Vomiting

Lead Sponsor:

Medical University of South Carolina

Conditions:

Obesity, Morbid

Postoperative Pain

Eligibility:

All Genders

18-80 years

Phase:

NA

Brief Summary

The purpose of this research study is to evaluate the drug gabapentin (Neurontin®) for its ability to reduce postoperative pain, the need for morphine-like pain medication, and the severity and freque...

Detailed Description

The occurrence of morbid obesity is at epidemic proportions in the United States. Laparoscopic gastric bypass is an effective means of safely facilitating patient weight loss and thereby drastically r...

Eligibility Criteria

Inclusion

  • Patients undergoing laparoscopic gastric bypass surgery
  • Age \> 18 years

Exclusion

  • Patients under the age of 18 years
  • Patients who undergo open gastric bypass
  • Patients with a history of chronic pain treated with pregabalin, gabapentin or opioids
  • Patients with a history of chronic renal disease (creatinine \> 1.3)
  • Patients with a history of bleeding gastric ulcer

Key Trial Info

Start Date :

February 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

January 1 2011

Estimated Enrollment :

62 Patients enrolled

Trial Details

Trial ID

NCT00886236

Start Date

February 1 2008

End Date

January 1 2011

Last Update

September 20 2018

Active Locations (1)

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Medical University of South Carolina

Charleston, South Carolina, United States, 29425