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Clinical Trial Summary

This study is a non-blinded randomized controlled trial comparing the use of a preoperative "mini" block plus postoperative local infiltration of Exparel (liposomal form of bupivacaine) versus a partial single shot nerve block in subjects undergoing primary reverse or total shoulder arthroplasty to see which is more effective in controlling surgery related pain. To do so, we will utilize the Visual Analog Scale (VAS) to measure pain intensity. Opioid consumption will be recorded on a Pain Monitoring Sheet.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03253198
Study type Interventional
Source Rothman Institute Orthopaedics
Contact
Status Completed
Phase N/A
Start date August 2016
Completion date July 2017

See also
  Status Clinical Trial Phase
Not yet recruiting NCT06464770 - Optimizing Infection Prophylaxis Prior to Shoulder Surgery N/A