Clinical Trials Directory

Trials / Completed

CompletedNCT01977352

Efficacy of Interscalene Brachial Plexus Block With Liposomal Bupivacaine for Arthroscopic Shoulder Surgery

Comparison of Cumulative Opioid Consumption After Interscalene Brachial Plexus Block With Liposomal Bupivacaine (Exparel; 88 mg in 20 cc) Versus Bupivacaine 0.25% for Arthroscopic Shoulder Surgery

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
42 (actual)
Sponsor
St. Luke's-Roosevelt Hospital Center · Academic / Other
Sex
All
Age
17 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to compare the quality and duration of pain relief after shoulder surgery provided by a single injection of liposomal bupivacaine versus standard bupivacaine when administered as an interscalene brachial plexus block. It is hypothesized that the liposomal bupivacaine formulation will provide more effective pain relief than standard bupivacaine.

Conditions

Interventions

TypeNameDescription
DRUGLiposomal bupivacaineliposomal bupivacaine (EXPAREL®; 88 mg in 20 cc)
DRUGBupivacaine 0.25%20 cc of bupivacaine 0.25%

Timeline

Start date
2014-01-01
Primary completion
2015-02-01
Completion
2015-02-01
First posted
2013-11-06
Last updated
2018-04-02
Results posted
2018-04-02

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01977352. Inclusion in this directory is not an endorsement.