Overview

Effectiveness of Intraoperative Exparel for Postoperative Pain Control in Total Knee Arthroplasty

Status:
Unknown status
Trial end date:
2016-06-01
Target enrollment:
0
Participant gender:
All
Summary
Does the use of periarticular Exparel in total knee arthroplasty prove to more effectively manage post operative pain control than another local analgesic, Ropivacaine, when both are used as part of a multimodal pain management approach? The investigators hypothesize that Exparel, a bupivacaine liposomal injectable suspension, will improve total knee arthroplasty postoperative pain with significant improvement of early function outcomes.
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
DeClaire LaMacchia Orthopaedic Institute
Treatments:
Bupivacaine
Epinephrine
Epinephryl borate
Ketorolac
Ketorolac Tromethamine
Morphine
Racepinephrine
Ropivacaine
Criteria
Inclusion Criteria:

- Patient undergoing Total Knee Arthroplasty with Dr. J.H. DeClaire

- 18 years of age or older

- Primary diagnosis of osteoarthritis of the knee

- Opioid naïve patient (according to FDA guidelines)

Exclusion Criteria:

- Prior knee replacement

- Prior use of narcotics for chronic pain management

- Inflammatory arthritis (Rheumatoid arthritis, Lupus, etc.)

- Unicompartmental knee replacement

- Bilateral Total Knee Arthroplasty

- Opioid Tolerant as defined by the FDA: Patients who are taking, for one week or
longer, at least:

> 60 mg oral morphine/day > 25μg transdermal fentanyl/hour > 30 mg oral oxycodone/day > 8
mg oral hydromorphone/day > 25 mg oral oxymorphone/day