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The Effect of EXPAREL® on Postsurgical Pain, and the Use of Narcotics

Rotator Cuff Tear Clinical Trial

Official title:
The Effect of EXPAREL® on Postsurgical Pain, and the Use of Narcotics

Clinical Trial Summary

Patients undergoing shoulder rotator cuff surgery in an outpatient setting are the focus of this study. The purpose of this study is to determine if the product EXPAREL® can be used as a safe alternative in shoulder surgery to pain pumps, while limiting narcotic use and providing appropriate postoperative pain control.

Clinical Trial Description

Based on prior research, it is hypothesized EXPAREL® can potentially be used as a local anesthetic option after undergoing an arthroscopic rotator cuff repair in the outpatient setting. Conducting this study, will allow the option for a surgeon to administer a local anesthetic, in a single injection, to the exact location of the surgical procedure and in a sterile environment. The purpose of this pilot study is to determine if EXPAREL® can be used as a safe alternative to current post-operative pain control methods, while limiting narcotic use and providing appropriate postoperative analgesia. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03290196
Study type Interventional
Source Andrews Research & Education Foundation
Contact
Status Suspended
Phase Phase 4
Start date September 3, 2015
Completion date July 2022
View Details
See also
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