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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

Conditions: Spine Surgery

Sex: All
Ages: 18 Years – 70 Years
Phase: PHASE2, PHASE3
Enrollment: 30
Sponsor: The University of Texas Health Science Center, Houston

Location: United States

Summary

The purpose of this study is to evaluate the feasibility and safety of a clinical protocol based on the administration of intraoperative intravenous methadone followed by a short regimen of oral/IV (if the patient is not able to take oral) methadone following spine surgery and to evaluate if methadone decreases persistent opioid usage at 3 months in comparison to placebo.

Eligibility Criteria

Inclusion Criteria:Adults undergoing multilevel complex lumbar and/or thoracic spine fusion surgery, including revision surgeriesExclusion Criteria:BMI greater than 40

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05693675). StuddyBuddy aggregates publicly available trial information.