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Study identifier: NCT04066296 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Outcomes for Lumbar Decompressions With Use of Liposomal Bupivicaine

Condition: Lumbar Spinal Stenosis  ·  Sponsor: University of Colorado, Denver

PhasePhase 2
Planned participants100
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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

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

Talk to the study team

Jens-Peter Witt, MD, PhD  ·  303-724-2306  ·  peter.witt@cuanschutz.edu

Akal Sethi, MD  ·  303-724-1995  ·  akal.sethi@cuanschutz.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Colorado Anschutz Medical CampusAurora, Colorado, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT04066296