LIBERATE - LIposomal Bupivacaine vERsus Adjuncts in Total shouldErs

Status Completed

Clinical Trial Summary

This will be a single-center, prospective, randomized controlled cross-sectional study comparing interscalene brachial plexus block with liposomal bupivacaine versus bupivacaine with epinephrine and PF dexamethasone in patients undergoing primary shoulder arthroplasty. Primary endpoint will be total opioid consumption in the first three post-operative days.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03887650
Study type	Interventional
Source	Hartford Hospital
Contact
Status	Completed
Phase	Phase 4
Start date	March 11, 2019
Completion date	March 8, 2022

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