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Clinical Trial Summary

The purpose of this study is to compare the effect of liposomal Bupivacaine infiltration into the shoulder to continues nerve block with Bupivacaine on postoperative pain control and functional outcomes.


Clinical Trial Description

liposomal bupivacaine analgesia will provide improved postoperative pain control, reduction in amount of opioid supplementation, decreased complications and faster return to function compared to current standard of care pain management for patients undergoing shoulder arthroplasty and shoulder surgery for proximal humerus fractures. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02472314
Study type Interventional
Source Wayne State University
Contact
Status Completed
Phase Phase 4
Start date June 2015
Completion date May 2017