Spine Surgery Clinical Trial
Official title:
Effect of Perioperative Intravenous Lidocaine Administration or Epidural Anesthesia on Postoperative Outcomes in Complex Spine Surgery
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.
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.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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