Expired Study
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Boston, Massachusetts 02120


Purpose:

The main objective of the study is to determine if intrarticular injection with liposomal bupivicaine (Exparel) provides better postoperative pain relief and functional outcome following total knee replacement (TKR) than the current standard New England Baptist Hospital regimen of femoral nerve block combined with intraarticular injection of a standard bupivicaine solution.


Study summary:

A prospective, single blind study comparing femoral nerve blockade and intraarticular posterior capsular injection to interarticular injection of bupivicaine and liposomal bupivicaine (Exparel) alone.


Criteria:

Inclusion Criteria: • Patients between the ages of 18 - 73 who are undergoing primary, unilateral, Total Knee Replacement at the New England Baptist Hospital in Boston, Massachusetts are eligible to participate. Exclusion Criteria: - Patients with Revision or Complex Total Knee Replacements and are under the age of 18, or over the age of 73 will be excluded. - Patients with an ASA 4 level will be excluded. - Patients with a Body Mass Index of less than 20, and over 40, will be excluded. - Patients taking preoperative narcotics, patients with extreme sensitivity or allergy to narcotics or local anesthetics, and patients using opioid medications for at least 3 months leading up to surgery, will also be excluded.


NCT ID:

NCT02473198


Primary Contact:

Principal Investigator
Carl Talmo, MD
New England Baptist Hospital


Backup Contact:

N/A


Location Contact:

Boston, Massachusetts 02120
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 21, 2017

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