The primary goal is to assess whether Lidocaine/IVPCA is better in morphine requirements and simultaneously not worse in pain control measured by VAS pain score compared to IVPCA alone.
Participants undergoing spine surgery will be randomized into one of three groups;General 1) Anesthesia and postoperative Patient Controlled Analgesia and placebo IV infusion,2) General Anesthesia plus perioperative intravenous lidocaine infusion and post operative patient controlled analgesia or 3) General Anesthesia plus postoperative epidural analgesia plus placebo IV infusion. After surgery, data will be collected including pain scores and narcotic and anesthesia requirements. Incidents of complications related to surgery or pain medications will be collected, such as bowel function, nausea and vomiting. Inflammatory mediators will be evaluated in all groups to determine anti-inflammatory effects.
Condition | Pain, Nausea, Vomiting, Wound Infection |
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Treatment | Placebo, lidocaine, propofol, or Etomidate, fentanyl |
Clinical Study Identifier | NCT00706524 |
Sponsor | Outcomes Research Consortium |
Last Modified on | 7 November 2020 |
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