RecruitingPhase 2NCT04066296

Outcomes for Lumbar Decompressions With Use of Liposomal Bupivicaine

A Double Blinded Randomized Control Trial in Outcomes for Lumbar Decompressions With Use of Liposomal Bupivicaine


Sponsor

University of Colorado, Denver

Enrollment

100 participants

Start Date

Sep 8, 2019

Study Type

INTERVENTIONAL

Conditions

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


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Liposomal bupivacaine for people with lumbar spinal stenosis. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGLiposomal bupivacaine

Injection of either liposomal bupivicaine or standard local anesthetic during surgical procedure.


Locations(1)

University of Colorado Anschutz Medical Campus

Aurora, Colorado, United States

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NCT04066296


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