Percutaneous periarticular analgesic injection at one day after total knee arthroplasty as a component of multimodal pain management: a randomized control trial
Not Applicable
- Conditions
- Osteoarthritis, Avascular necrosis of femoral condyle, Rheumatoid arthritis
- Registration Number
- JPRN-UMIN000029003
- Lead Sponsor
- ekoyama Miyao Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
Patients scheduled for simultaneous bilateral total knee arthroplasty. Patients scheduled for unilateral total knee arthroplasty combined with implant removal. Patients who had allergy or intolerance to one of the study drugs. Patients who had poorly controlled diabetic mellitus.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual Analogue Scale for postoperative pain at rest measured at 12:00 and 20:00 of one day after surgery, and 6:00, 12:00, and 20:00 of two to five days after surgery.
- Secondary Outcome Measures
Name Time Method Complication Visual Analogue Scale during activity (measured at one to five days after surgery) Range of knee movement (measured at one to five days after surgery)