The Effect of Zolpidem on Outcomes Following Lumbar Spine Fusion

Status Recruiting

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

Clinical Trial Details

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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