Effect of duloxetine on postoperative pain after high tibial osteotomy: a randomized controlled trial
Not Applicable
- Conditions
- knee osteoarthritis
- Registration Number
- JPRN-UMIN000040026
- Lead Sponsor
- Ogaki Tokushukai Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 82
Inclusion Criteria
Not provided
Exclusion Criteria
patients who took duloxetine within 1 month.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain VAS
- Secondary Outcome Measures
Name Time Method