Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of Tennessee
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Age \> 18 years
ASA physical status 1-3
Undergoing either carpometacarpal arthroplasty or proximal row carpectomy operation
Physically and mentally able to participate in the study and complete all study assessments
Able to voluntarily give fully informed consent to participate in this study and complete all study assessments within the timeframes required.
You may not be if
History of hypersensitivity or idiosyncratic reactions to amide-type local anesthetics
Any patient whose anatomy, or surgical procedure, in the opinion of the Investigator, might preclude the potential successful local administration of EXPAREL
Patients who have received any investigational drug within 30 days prior to EXPAREL administration, or planned administration of another investigational product or procedure during their participation in this study
Any chronic condition requiring use of opioids for treatment of the medical condition for three (3) months or more
Confirmed pregnancy at time of enrollment
Patients unable to comply with the study requirements, i.e. inaccessible by phone, or deaf
