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Study identifier: NCT07517679 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Methadone for Post-operative Spine Surgery

Condition: Pain, Postoperative  ·  Sponsor: Brandon Knopp

PhasePhase 4
Planned participants30
Who can joinAll sexes, 18 Years to 120 Years
Healthy volunteersNo

About this study

The goal of this prospective cohort study is to evaluate the clinical effects of post-induction methadone on perioperative pain control, opioid requirements, and recovery outcomes in adult patients undergoing elective spine surgery, with the goal of improving postoperative analgesia and enhancing recovery efficiency. The main questions it aims to answer are the perioperative pain control and opioid requirements between the two groups. Post-induction methadone can offer equivalent or improved pain control following major spine procedures and reduce intra- and postoperative opioid requirements, improve perioperative pain control and shorten PACU stay. Researchers will compare perioperative opioid use (morphine equivalents (ME), during the intraoperative and postoperative periods (PACU and 24-hour totals) between the standard intraoperative opioid regimen group and the methadone group. Patients will be randomized preoperatively to one of two groups: (both groups will receive additional multimodal pain control including opioids, not including methadone, as needed) Standard intraoperative opioid regimen (control) Methadone 0.2 mg/kg (max 20 mg) If the patient is in the methadone group, the patient will receive a predetermined dose of Methadone (0.2mg/kg) intravenously after induction (they are given medications to sleep for surgery). They will proceed with surgery, and all patients will receive standard of care management regardless of whether they receive Methadone or not. Fo…

This description comes directly from the study's public registry record.

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Locations (1)

University of KentuckyLexington, Kentucky, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07517679