Femoral Nerve Block Compared to Exparel in Total Knee Replacement
Launched by THE NEW ENGLAND BAPTIST HOSPITAL · Jun 15, 2015
Trial Information
Current as of April 30, 2025
Unknown status
Keywords
ClinConnect 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.
Gender
ALL
Eligibility 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.
About The New England Baptist Hospital
New England Baptist Hospital (NEBH) is a leading healthcare institution specializing in orthopedic care and musculoskeletal health. With a commitment to advancing medical knowledge and improving patient outcomes, NEBH conducts clinical trials that explore innovative treatment options and therapeutic interventions. The hospital's dedicated research team collaborates with clinicians and scientists to ensure rigorous study design and ethical standards, providing patients access to cutting-edge therapies while contributing to the broader medical community's understanding of orthopedic conditions. Through its research initiatives, NEBH aims to enhance evidence-based practices and foster advancements in orthopedic medicine.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Boston, Massachusetts, United States
Patients applied
Trial Officials
Carl Talmo, MD
Principal Investigator
New England Baptist Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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