Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is determine if epidural anesthesia administered after surgery or lidocaine administered during surgery will decrease inflammation after spinal surgery and decrease the need for post operative pain medication compared to intravenous patient controlled analgesia. Participants undergoing spine surgery will be randomized into one of two groups;

- A.) General Anesthesia and postoperative Patient Controlled Analgesia and placebo IV infusion.

B.) General Anesthesia plus perioperative intravenous lidocaine infusion, and post operative Patient Controlled Analgesia.


Clinical Trial Description

According to a survey of 1570 U.S neurosurgeons, in the United States about 527.000 spine surgeries were done in 1999. This represents close to 65% of the procedures performed by neurosurgeons. Furthermore, the number of hospitalizations related with spine surgery has significantly increased since 1970.

IV PCA is considered the standard of care for postoperative pain control after surgery. Intravenous opioids have significant side effects such as respiratory depression, postoperative nausea and vomiting and sedation. Furthermore, they cause delayed return of bowel function and ileus.

There is the possibility of surgically inserting a catheter into the epidural space at the end of surgery. In general epidural analgesia provides excellent pain relief after surgery and decreases opioid consumption significantly und thus opioid related postoperative complications. Furthermore epidural anesthesia affects the surgical stress response and might decrease inflammatory responses after surgery, thereby improving postoperative recovery and mobilization of the patients.

Intravenous local anesthetics have potent anti-inflammatory properties. They also decrease postoperative opioid consumption. Clinical studies have shown that perioperative local anesthetic administration significantly reduces the incidence of thrombosis and postoperative pain, shortens postoperative ileus and decreases duration of hospitalization. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00840996
Study type Interventional
Source Outcomes Research Consortium
Contact
Status Completed
Phase N/A
Start date May 2008
Completion date February 2012

See also
  Status Clinical Trial Phase
Completed NCT00967109 - Establishment of Optimal Transfusion Threshold During Spine Surgery N/A
Terminated NCT00805844 - Motor Evoked Potentials and SedLine N/A
Terminated NCT05494125 - Effects of Continuous ESP Catheters on Recovery, Pain and Opioid Consumption After Multilevel Spine Surgery N/A
Recruiting NCT06210061 - Propofol-Fentanyl-Dexmedetomidine and Propofol-Fentanyl-Sevoflurane Anesthesia for Major Spine Surgery Under Somato Sensory- and Motor- Evoked Potential Monitoring N/A
Completed NCT05016739 - Use of CADISS Medical Device to Facilitate Dissection of Epidural Fibrosis in Revision Spine Surgery N/A
Not yet recruiting NCT05478382 - Pregabalin is an Effective Treatment for Acute Postoperative Pain Following Spinal Surgery Without Major Side Effects Phase 4
Not yet recruiting NCT05015036 - Evaluation of an Enhanced Recovery Protocol After Minimally Invasive Lumbar Surgery.
Not yet recruiting NCT02551302 - "Efficacy of Hybrid Systems ("Topping Off") Versus Rigid Spinal Fusion in Lumbar Fusion Surgery: A Dual-center, Prospective, Randomized Pilot Study ("CD Horizon BalanC")" N/A
Not yet recruiting NCT05693675 - Postoperative Oral Methadone After Major Spine Surgery; Safety, Feasibility and Efficacy in Prevention of Progression to Chronic Opioid Usage at 3 Months Phase 2/Phase 3
Completed NCT02884440 - Transverse Abdominis Plane Block for Anterior Approach Spine Surgery Phase 2
Completed NCT04574388 - Evaluation of Open-Label Conditioned Placebo Analgesia for Postoperative Opioid Reduction Following Spinal Fusion N/A
Completed NCT02949518 - Enhanced Recovery After Spine Surgery N/A
Completed NCT04473508 - Erectus Nerve Block for Lumbar Spine Surgery Phase 3
Recruiting NCT05131854 - Incidence , Risk Factors and Outcomes of Haemodynamic Instability and Cardiac Arrest During Spine Surgery
Completed NCT03112993 - Speed of Recovery of Reversal of Neuromuscular Blockade in Geriatric Patients Undergoing Spine Surgery Phase 4
Terminated NCT00696501 - Direct Stimulation Of Spinal Nerve Roots To Determine Sensory And Motor Innervation Patterns N/A
Recruiting NCT05626868 - Changes of Intra Abdominal Pressure During Surgeries in Prone Position as a Marker of Renal Damage
Recruiting NCT04797156 - Combined IV and Topical TXA in Major Spine Surgery Early Phase 1
Completed NCT02606695 - Comprehensive Spinal Alignment Planning Study
Recruiting NCT04574778 - Randomized Trial of Intraoperative IV Versus Preoperative Oral Acetaminophen During Ambulatory Lumbar Discectomy Phase 3