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

NCT03159130 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2017-05-18

No results posted yet for this study

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.

Conditions

  • Morbid Obesity

Sponsors & Collaborators

  • William Beaumont Army Medical Center

    lead FED

Principal Investigators

  • Gregory Peirce, MD · William Beaumont Army Medical Center

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-06-30
Primary Completion
2014-06-30
Completion
2014-06-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03159130 on ClinicalTrials.gov