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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

18-75 Years
18 to 99 Years
All
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?

Yes

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.

No

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.

Locations

Location

Status