Overview

Local Infiltration With Bupivacaine to Increase Quality of Post-operative Pain Control in Total Knee Replacement

Status:
Completed
Trial end date:
2010-09-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to evaluate the efficacy of periarticular injection with 0.25% bupivacaine for controlling pain after total knee replacement to improve the quality of post-operative care.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Mahidol University
Collaborator:
Siriraj Hospital
Treatments:
Bupivacaine
Criteria
Inclusion Criteria:

- primary osteoarthritis patients undergoing total knee replacement at Siriraj Hospital

- BMI between 20-35

- having a full understanding of the question in this trial

Exclusion Criteria:

- allergy to NSAIDs, Acetaminophen, Bupivacaine

- blood creatinine more than 1.5 mg/dl or creatinine clearance less than 60 mL/min

- abnormal liver function

- previous surgery on the knee undergoing total knee replacement

- patient could not receive spinal anesthesia