Exparel Use in Adductor Canal Block After Total Knee Arthroplasty
Sponsored by St. Luke's Hospital, Pennsylvania
About this trial
Last updated 3 years ago
Study ID
SLIR 2019-106
Status
Completed
Type
Interventional
Phase
Phase 3
Placebo
No
Accepting
18 to 99 Years
All
Trial Timing
Ended 4 years ago
What is this trial about?
Exparel has been shown to have better pain control compared to previously used infiltration
agents, including bupivacaine, while having a minor side effect profile. The purpose of this
study is to explore the effectiveness of Exparel (liposomal bupivacaine) in Adductor Canal
Blocks for peri-operative pain control following a total knee arthroplasty (TKA) procedure.
What are the participation requirements?
Inclusion Criteria
- Patients were eligible for inclusion if they were undergoing unilateral primary TKA for a diagnosis of knee osteoarthritis and were not undergoing any additional concomitant procedures were.
Exclusion Criteria
- Patients were not eligible for our study if they were undergoing revision TKA, if they were undergoing bilateral TKA or concomitant procedures, or if they had an active infection.