Overview

Local Infiltration Analgesia During Total Knee Arthroplasty

Status:
Unknown status
Trial end date:
2012-12-01
Target enrollment:
0
Participant gender:
All
Summary
The primary objective is to evaluate whether local infiltration analgesia (LIA) will reduce oxycodone consumption during the first 48 postoperative hours in patients undergoing total knee arthroplasty (TKA).
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Coxa, Hospital for Joint Replacement
Treatments:
Bupivacaine
Epinephrine
Epinephryl borate
Ketorolac
Ketorolac Tromethamine
Levobupivacaine
Racepinephrine
Criteria
Inclusion Criteria:

- Patients requiring primary TKA for primary OA

- Patients aged 75 years or less

- Patients suitable for all applicable devices

Exclusion Criteria:

- Rheumatoid arthritis or other inflammatory diseases

- Patients requiring bone grafting during surgery

- Unwilling to provide informed consent

- BMI > 35

- ASA > 3

- Renal dysfunction

- Allergic to ASA

- Previous high tibial osteotomy or previous osteosynthesis

- > 15 degrees varus / valgus malalignment

- Physical, emotional or neurological conditions which would comprise the patient´s
compliance with postoperative rehabilitation and follow-up (e.g. drug or alcohol
abuse, serious mental illness, general neurological conditions such as Parkinson, MS,
etc.)

- Known sensitivity to materials in the devices