Preventive injection of some types of pain-relief drugs around knee joint for management of pain after complete replacement of knee joint.
Not Applicable
- Conditions
- Condition 1: Arthrosis of knee (Gonarthrosis). Condition 2: Severity of pain after Total Knee Arthroplasty. Condition 3: Total Knee Arthroplasty.Other primary gonarthrosisOther complications of internal orthopaedic prosthetic devices, implants and graftsPresence of other specified functional implants
- Registration Number
- IRCT2016073129132N2
- Lead Sponsor
- Isfahan University of Medical Sciences and Health Cares.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
individuals with osteoarthritis who were scheduled for primary unilateral TKA.
Exclusion criteria: BMI greater than 40; previous history of allergy to any medications; known abuser of alcohol and other drugs; any inflammatory arthritis; previous major surgery in the same knee joint indicated for TKA; individuals who were candidated for bilateral TKA; patients who did not show up for the follow-up.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The severity of the pain in knee joint. Timepoint: 24 hours, 48 hours and 6 weeks after the surgery. Method of measurement: Visual Analog Scale (VAS).
- Secondary Outcome Measures
Name Time Method Function of knee joint. Timepoint: 6 weeks and 6 months after surgery. Method of measurement: Knee Society Score.