Ketamine in Orthopedic Trauma: Potential to Reduce Pain and Opioid Use
This ongoing Phase 4 clinical trial, sponsored by Texas Tech University Health Sciences Center, aims to evaluate the efficacy of intraoperative ketamine in improving recovery outcomes for adults undergoing orthopedic trauma surgery. The study enrolls 90 participants, who are randomly assigned to receive either a single dose of ketamine or standard general anesthesia during surgery. The primary endpoint is postoperative pain intensity, assessed using the Visual Analog Scale (VAS). Secondary endpoints include opioid consumption, as well as mental health outcomes measured by the PHQ-9 for depression and PCL-5 for PTSD. Participants' opioid prescriptions will be monitored through electronic medical records, and follow-up assessments will occur at multiple time points up to 6 months post-surgery. While ketamine is known for its anesthetic properties, it may offer additional benefits in reducing acute pain, decreasing opioid requirements, and improving depressive symptoms. The study's findings could inform new approaches to managing both physical and psychological recovery in this patient population. Safety and adverse event data will be collected, though specific statistics and outcomes are not yet available.