Serum Levels of Bupivacaine in Autotransfusion Drains Following Total Joint Arthroplasty

CompletedOBSERVATIONAL
Enrollment

26

Participants

Timeline

Start Date

October 31, 2014

Primary Completion Date

June 30, 2015

Study Completion Date

June 30, 2017

Conditions
Knee Pain Arthritis
Interventions
DRUG

periarticular bupivicaine and liposomal bupivicaine

Participants will receive Exparel (liposomal bupivacaine). Exparel is a FDA approved product. Exparel is an extended-release formulation of bupivacaine consisting of microscopic lipid-based particles that diffuse over an extended period. The result is pain relief that can last up to 96 hours after surgery. Extended-release liposomal bupivacaine-based analgesics were shown to provide extended pain relief and decrease opioid (pain medication) use. At the conclusion of the total joint arthroplasty procedure, Exparel is administered via injection into the joint (periarticular bupivicaine and liposomal bupivicaine).

Trial Locations (4)

28207

OrthoCarolina, PA, Charlotte

28209

Novant Health Charlotte Orthopedic Hospital, Charlotte

OrthoCarolina Research Institute, OrthoCarolina, P.A., Charlotte

OrthoCarolina, PA, Charlotte

All Listed Sponsors
lead

OrthoCarolina Research Institute, Inc.

OTHER

NCT02276040 - Serum Levels of Bupivacaine in Autotransfusion Drains Following Total Joint Arthroplasty | Biotech Hunter | Biotech Hunter