Clinical Trials Directory

Trials / Completed

CompletedNCT01983020

Peri-Operative Lidocane, Ketamine, or Lidocane and Ketamine Combination, Infusion for Patients Undergoing Spine Surgery

Randomized Double Blind Comparison of Peri-Operative Standard Analgesia With Peri-Operative Lidocane, Ketamine, or Lidocane and Ketamine Combination, Infusion for Patients Undergoing Spine Surgery

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
46 (actual)
Sponsor
Beth Israel Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study has been designed as a controlled clinical trial to evaluate the efficacy of brief lidocaine infusion, brief ketamine infusion and a lidocaine/ketamine combined infusion when added to conventional opioid therapy following major spine surgery, as well as to evaluate the effects of the lidocaine/ketamine pain protocol on the feasibility of performing routine intraoperative neurophysiology during spine surgery in adults and determine whether this infusion protocol is compatible with intraoperative neurophysiology on spine surgery patients. If one or more of the approaches is confirmed as efficacious and safe, it could have a significant impact on the routine management of postoperative pain in this context.

Conditions

Interventions

TypeNameDescription
DRUGLidocaine
DRUGKetamine
OTHERSaline

Timeline

Start date
2011-04-01
Primary completion
2013-01-01
Completion
2013-01-01
First posted
2013-11-13
Last updated
2017-05-15
Results posted
2017-05-15

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01983020. Inclusion in this directory is not an endorsement.