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OnQ Pain Pump Effectiveness in Post Operative Pain Control in Bariatric Patients

Morbid Obesity Clinical Trial

Official title:
OnQ Pain Pump Effectiveness in Post Operative Pain Control in Bariatric Patients

Clinical Trial Summary

This study will assess the efficacy of OnQ pain catheters in pain reduction in the bariatric surgical population and seeks to identify if a quantifiable improved post-operative course occurs in patients receiving a catheter filled with local anesthetic versus that achieved by patients who receive a catheter filled with injectable saline.

Clinical Trial Description

This study will assess the efficacy of OnQ pain catheters in pain reduction in the bariatric surgical population. Approximately 12 to 15 weight reduction surgeries are performed at William Beaumont Army Medical Center each month. It is the current practice that each patient receiving the laparoscopic gastric sleeve or laparoscopic Roux-en-Y gastric bypass receive an OnQ pain catheter during the surgery to reduce post-operative pain. There have been limited studies to quantify the efficacy of these devices. This study will seek to identify if a quantifiable improved post-operative course occurs in patients receiving a catheter filled with local anesthetic versus that achieved by patients who receive a catheter filled with injectable saline. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03159130
Study type Observational
Source William Beaumont Army Medical Center
Contact
Status Withdrawn
Phase N/A
Start date June 2012
Completion date June 2014
View Details
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