Clinical Trials Directory

Trials / Completed

CompletedNCT02472314

Exparel for Postoperative Pain Management in Shoulder Surgery

A Novel Application of Exparel for Postoperative Pain Management in Shoulder Arthroplasty and Humerus Fracture Fixation

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
70 (actual)
Sponsor
Wayne State University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUG1.3% Liposomal Bupivacainelocal tissue infiltration of Liposomal Bupivacaine during surgery
DRUG0.125% BupivacaineContinues nerve block with Bupivacaine during surgery and postoperatively

Timeline

Start date
2015-06-01
Primary completion
2017-05-01
Completion
2017-05-01
First posted
2015-06-15
Last updated
2023-12-29
Results posted
2019-04-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02472314. Inclusion in this directory is not an endorsement.