Effectiveness of a Femoral Block Following Total Knee Arthroplasty (TKA)

Edmonton Civic Employees Research Fund

Status and phase: Completed; Phase 4

Conditions: Total Knee Arthroplasty

Treatments: Other: Usual Care; Procedure: Femoral Block

Study type: Interventional

Funder types: Other

Identifiers

NCT00659087

J-3224

Details and patient eligibility

About

Hospital stays after total joint replacement surgery have been getting shorter over the past 10 years. This is mostly due to new ways to manage pain and early rehabilitation. To be able to go home safely soon after surgery, patients need to:

• 1. have adequate pain control
• 2. be able to move through activities of daily living on their own (using aids)

Femoral nerve block, in combination with pain medications, is one of the new treatment strategies that are currently being used at other hospitals in Canada, the United States and the United Kingdom. Nerve blocks involve a needle filled with local anesthetic into the nerve that allows the feeling of pain around the knee. With good pain management, patients will be able to more quickly bend their knee and regain the ability to walk with aids and move from sitting and lying positions to standing and walking. Once they can do these activities with adequate pain control, they can be discharged from hospital to continue recovery at home. The purpose of this study is to examine a new way of managing postoperative pain and encourage early knee flexion and mobility, while maintaining pain control for patients after total knee replacement. We believe that patients who receive the nerve block in addition to the regular pain medication will have more knee flexion at discharge and experience less pain than patients who only receive usual pain medications.

Enrollment: 20 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Undergoing primary total knee arthroplasty
• English-speaking
• Preoperative knee ROM > 90 degrees
• Body Mass Index < 40

Exclusion criteria

• Regular preoperative opioid use
• Hepatic insufficiency
• Any contra-indications to receiving a femoral block

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: Single Blind

---

20 participants in 2 patient groups

Femoral Block

Experimental group

Description:

Those receiving femoral block in addition to usual pain management

Treatment:

Procedure: Femoral Block

Usual Care

Active Comparator group

Description:

Those receiving only usual pain management without a femoral block

Treatment:

Other: Usual Care