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Clinical Trial Summary

The purpose of this study is to evaluate if peri-operative zolpidem for posterior lumbar spinal fusion improves patient reported outcomes following surgery.


Clinical Trial Description

Patients who are undergoing one- to three-level spinal fusion for degenerative lumbar disease will be recruited. They will be randomized to either receive zolpidem or placebo two days preoperatively and five days postoperatively. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05746143
Study type Interventional
Source University of Southern California
Contact Pui Yan, MS
Phone 323-442-6984
Email puiyan@med.usc.edu
Status Recruiting
Phase N/A
Start date February 1, 2022
Completion date December 31, 2025

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