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Liposomal bupivacaine for Pain relief
Phase 3
Waitlist Available
Led By Donald A Elmer, MD
Research Sponsored by University of Virginia
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 72 hours postoperative
Awards & highlights
Study Summary
This study is evaluating whether a combination of liposomal bupivacaine and bupivacaine is more effective than plain bupivacaine for interscalene nerve block.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 72 hours postoperative
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~72 hours postoperative
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Opioid Consumption
Secondary outcome measures
Nerve Block Related Adverse Events
Numeric Rating Scale Reported Pain Scores
Patient Reported Satisfaction with Postoperative Pain Control Using the Numeric Rating Scale
+1 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Liposomal BupivacaineExperimental Treatment2 Interventions
Experimental group will receive ISNB with admixed LB (10 mL) and 0.5% bupivacaine (10 mL) total of 20 mL.
Group II: Non-liposomal BupivacaineActive Control1 Intervention
Comparator group will receive ISNB with 20 mL of 0.5% non-liposomal bupivacaine
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Liposomal bupivacaine
2016
Completed Phase 4
~1970
Bupivacaine
2013
Completed Phase 4
~1530
Find a Location
Who is running the clinical trial?
University of VirginiaLead Sponsor
753 Previous Clinical Trials
1,244,954 Total Patients Enrolled
Donald A Elmer, MDPrincipal InvestigatorUniversity of Virginia
Frequently Asked Questions
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