Comparison of the effect on the postoperative pain between intravenous acetaminophen and flurbiprofen after total knee arthroplasty: a randomized controlled trial
Not Applicable
- Conditions
- Osteoarthritis of the knee
- Registration Number
- JPRN-UMIN000029487
- Lead Sponsor
- agasaki Rosai Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 75
Inclusion Criteria
Not provided
Exclusion Criteria
1. ASA physical status 3-6 2. Liver or renal dysfunction 3. Past history of peptic ulcer or asthma 4. Allergy to acetaminophen or NSAIDs or local anesthetics
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain evaluated by Numerical Rating Scale (NRS) during first 24 h after total knee arthroplasty.
- Secondary Outcome Measures
Name Time Method