Outcomes for Lumbar Decompressions With Use of Liposomal Bupivicaine

Status Recruiting

Clinical Trial Summary

Evaluate the benefit of using liposomal bupivicaine in lumbar laminectomies in terms of length of stay, IV narcotic use, 30-day narcotic use, visual analog score (VAS) and 30-day readmissions

Clinical Trial Description

Recent evidence suggests the use of liposomal bupivicaine (LB) in lumbar spine surgery shortens length of hospital stay and overall post-operative narcotic use. Studies have shown its utility in single level microdiscectomies and lumbar fusions, but there have been no publications regarding lumbar laminectomies and associated outcomes with LB. The investigators' hypothesis is that LB will significantly shorten inpatient stays as well as overall narcotic usage in single, double or multi-level lumbar laminectomies. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04066296
Study type	Interventional
Source	University of Colorado, Denver
Contact	Jens-Peter Witt, MD, PhD
Phone	303-724-2306
Email	peter.witt@cuanschutz.edu
Status	Recruiting
Phase	Phase 2
Start date	September 8, 2019
Completion date	January 2024

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