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
| Type | Name | Description |
|---|---|---|
| DRUG | Lidocaine | |
| DRUG | Ketamine | |
| OTHER | Saline |
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.