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

Withdrawn before enrolling

Conditions studied: Morbid Obesity

In brief

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.

Key facts

Study ID

NCT03159130

Run by

William Beaumont Army Medical Center

People needed

0

Starts

2012-06-01

Expected to finish

2014-06-01

Last updated by the study team

2017-05-18

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Meets criteria for Bariatric surgery
• Consents to be in protocol
• No local anesthetic allergy
• Will be having sleeve gastrectomy
• Doesn't have extensive scarring of abdominal wall that would prevent placement of OnQ catheter

You may not qualify if…

• declines to participate

Where it is running

• William Beaumont Army Medical Center — El Paso, Texas, United States

Full record on ClinicalTrials.gov

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