Post-operative Exparel Study Following Rotator Cuff Repair

Status Not yet recruiting

Clinical Trial Summary

The primary purpose of this study is to determine if the postoperative oral narcotics consumption in patients receiving liposomal bupivacaine (LB) interscalene brachial plexus nerve block (ISBPB) is different than the narcotics consumption receiving traditional bupivacaine ISBPB for arthroscopic rotator cuff repair analgesia.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04047745
Study type	Interventional
Source	Rothman Institute Orthopaedics
Contact	Director of Clinical Trials
Phone	267-339-7818
Email	tiffany.morrison@rothmanortho.com
Status	Not yet recruiting
Phase	N/A
Start date	September 2019
Completion date	September 2021

View Details

See also
Status	Clinical Trial	Phase
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