The opportune time for periarticular injection during total knee arthroplasty under general anesthesia: a randomized controlled trial
Not Applicable
- Conditions
- Osteoarthritis of the knee, rheumatoid arthritis, avascular necrosis
- Registration Number
- JPRN-UMIN000021910
- Lead Sponsor
- Hokusuikai Kinen 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 who had allergy or intolerance to one of the study drugs, regular narcotic use, renal insufficiency and prolonged QT interval on ECG.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method