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Clinical Trial Summary

The goal of this research proposal is to determine if the intraoperative administrative of Ketamine and Magnesium during laparoscopic gynecologic surgery improves postoperative pain in patients on chronic opioid therapy for management of chronic pelvic pain.


Clinical Trial Description

In this randomized control trial, patients' postoperative pain scores will be assessed as scored by the Numeric Rating Score (NRS) system. Intraoperative and postoperative narcotic usage, nausea scores and patients' perception of their quality of recovery via the QoR-40 survey will also be assessed. The use of intraoperative Ketamine and Magnesium is predicted to decrease postoperative pain in patients on chronic opioid therapy for management of chronic pelvic pain and will overall improve patients' postoperative experience. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02940509
Study type Interventional
Source Milton S. Hershey Medical Center
Contact
Status Terminated
Phase Phase 1
Start date July 1, 2017
Completion date February 27, 2018

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