Overview

Liposomal Bupivacaine Versus Interscalene Nerve Block

Status:
Recruiting
Trial end date:
2021-12-01
Target enrollment:
0
Participant gender:
All
Summary
The aim of this study is to compare two different pain management interventions in patients undergoing reverse total shoulder arthroplasty. The two interventions are 1) pre-operative interscalene nerve block and 2) intraoperative injection of liposomal bupivacaine (Exparel, Pacira Pharmaceuticals, Parsippany NJ). Specifically, the primary aims of this study are to compare these two interventions on the following: post-operative opioid consumption, pain scores, and patient satisfaction. Additionally, the investigators want to determine if psychological factors, catastrophizing and resilience, are associated with post-operative pain control and satisfaction. The investigators' hypothesis is that the two interventions will have similar pain control efficacy and that the liposomal bupivacaine group will experience faster post-operative recovery, earlier discharge, and improved satisfaction. The investigators also expect patient catastrophizing and resilience to significantly predict the degree of post-operative pain and level of patient satisfaction.
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
University of Cincinnati
Treatments:
Bupivacaine
Criteria
Inclusion Criteria:

- patients who are older than 18 years

- patients undergoing reverse total shoulder arthroplasty

Exclusion Criteria:

- pregnancy

- inability to provide informed consent

- deemed unreliable for follow-up survey completion

- individuals who do not speak English

- those who have an allergy to the study medications (ropivicaine, bupivicaine) or have
clinically significant hepatic disease