Clinical Trials Directory

Trials / Completed

CompletedNCT03738696

Liposomal Bupivacaine in Rotator Cuff Repair

Efficacy of Liposomal Bupivacaine in Arthroscopic Rotator Cuff Repair

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
64 (actual)
Sponsor
University of Alabama at Birmingham · Academic / Other
Sex
All
Age
19 Years
Healthy volunteers
Not accepted

Summary

To assess the efficacy of interscalene liposomal bupivacaine in controlling postoperative pain scores, oral morphine equivalents and sleep quality after arthroscopic rotator cuff repair surgery as compared to interscalene catheter.

Conditions

Interventions

TypeNameDescription
DRUGExparelA long-acting injectable sodium channel blocker bound to lipid that is indicated in controlling postoperative pain
DRUGRopivacaineA short-acting injectable sodium channel blocker bound to lipid that is indicated in controlling postoperative pain

Timeline

Start date
2019-12-15
Primary completion
2022-01-01
Completion
2022-01-01
First posted
2018-11-13
Last updated
2024-05-16
Results posted
2024-05-16

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03738696. Inclusion in this directory is not an endorsement.