Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT02426164

Liposomal Bupivacaine in Total Knee Arthroplasty

Analgesic Efficacy of Liposomal Bupivacaine in Total Knee Arthroplasty

Status
Withdrawn
Phase
Phase 4
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Miller Orthopedic Specialists · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Liposomal bupivacaine is a novel local anesthetic designed for prolonged pain relief. Despite its long-acting analgesic potential, liposomal bupivacaine is significantly more expensive than other local anesthetic alternatives. The primary aim of this investigation is to examine whether or not liposomal bupivacaine provides superior pain relief or clinically significant opioid-sparing effects versus a control to justify its cost.

Conditions

Interventions

TypeNameDescription
DRUGLiposomal bupivacainePeriarticular infiltration of the liposomal bupivacaine with 20cc of normal saline
DRUGbupivacaine HCl, morphine, epinephrine, methylprednisolonePeriarticular infiltration of 24c of bupivacaine HCl, 0.8cc morphine, 0.3cc epinephrine, and 1cc of methylprednisolone

Timeline

Start date
2015-06-01
Primary completion
2017-06-01
Completion
2017-06-01
First posted
2015-04-24
Last updated
2016-03-22

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02426164. Inclusion in this directory is not an endorsement.