Clinical Trials Logo

Clinical Trial Summary

The purpose of this research is to determine the pain-reducing effects of ketamine (Ketalar, an FDA-approved drug for anesthesia) and methadone (Dolophine, a long-acting narcotic) after lumbar laminectomy. The investigators would like to evaluate whether intraoperative use of both drugs may be able to provide better control of pain after lumbar surgery.


Clinical Trial Description

During and after the surgery, patients undergoing surgery most likely need narcotics (opioids) that can cause side effects such as drowsiness and constipation. This can delay your recovery. The investigator would like to determine if the intraoperative use of ketamine and methadone will provide better pain control and reduce the use of narcotic painkiller medications (analgesics) after lumbar surgery as compared to either drug (ketamine or methadone) alone. Ketamine is used to help to reduce the amount of the commonly used intravenous anesthetic drugs, minimize heart rate and blood pressure instability during surgery, and to improve outcomes after surgery (e.g. less pain, less constipation, less nausea and vomiting after surgery, faster return of bowel function and shortened length of hospital stay). Ketamine is approved by the U.S. Food and Drug Administration (FDA) to be used: as an anesthetic and analgesic (painkiller). Ketamine is an "adjuvant," which is a drug that may increase the effectiveness or strength of other drugs when given at the same time. Ketamine is administered as an adjuvant during anesthesia to produce anesthetic and analgesic-sparing effects (reduce the amount of anesthetics and narcotics-painkiller drugs), hemodynamic stability (to maintain the blood pressure and heart rate within normal rank) and side effect reduction (e.g., constipation, nausea and vomiting, itching, and urinary retention). Ketamine will be used as approved in this study. Ketamine is frequently used intraoperatively for pain control in patients undergoing spine surgery at our institution and is within the standard of care. The standard of care indicates that this is one possible method which has been demonstrated to be safe and effective for patient care. This may vary at different institutions. Methadone is approved by the U.S. Food and Drug Administration (FDA) to be used: as an opioid pain reliever, similar to morphine, and for narcotic detoxification to reduce withdrawal symptoms. The dose of methadone that will be used in this study may be slightly higher than the approved dose depending on the subject's weight. However, this dose of methadone is frequently used intraoperatively for pain control in patients undergoing spine surgery at our institution and is within the standard of care. This may vary at different institutions. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02252432
Study type Interventional
Source Cedars-Sinai Medical Center
Contact
Status Terminated
Phase Phase 4
Start date February 2013
Completion date January 2023

See also
  Status Clinical Trial Phase
Completed NCT00656526 - Preemptive Analgesia for Postlaminectomy Phase 4
Completed NCT03702010 - Spinal Cord Stimulation in Patients With Post-Laminectomy Syndrome in Testing Phase N/A
Not yet recruiting NCT06358040 - Opioid Dispenser for Microdiscectomy/Laminectomy N/A
Completed NCT04498338 - Neural Mobilization and Conventional Physical Therapy After Laminectomy N/A
Terminated NCT01179113 - Esmolol Infusion During Laminectomy: Effect on Quality of Recovery Phase 4
Recruiting NCT00518544 - Hemostatic Effect of Various Colloid Solutions N/A
Completed NCT04981158 - Enhanced Recovery After Lumber Laminectomy Using Epidural and General Anesthesia N/A
Completed NCT05525052 - Percutaneous Trans-facet Screw Fixation Under CT-scan Guidance for Remaining Symptoms at a Distance of Previous Spinal Surgery
Completed NCT01113723 - Intubation of Patients With an Unstable Cervical Spine Using the CMAC Device Phase 4