Comparison of patient-controlled analgesia with background opioid versus non-opioid infusion for postoperative pain in patients undergoing total knee arthroplasty
Not Applicable
Recruiting
- Conditions
- Diseases of the musculoskeletal system and connective tissue
- Registration Number
- KCT0008154
- Lead Sponsor
- Chung-Ang University Gwangmyeong Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 98
Inclusion Criteria
We will enrolled patients aged 60-78 years with ASA physical status I–II, and undergoing elective total knee arthroplasty under spinal anesthesia.
Exclusion Criteria
We will exclude patients with risk of complications associated with fentanyl, ketorolac, and nefopam.
Those who are contraindicated to undergo spinal anesthesia will be also excluded.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome is the pain score evaluated by visual analogue scale 24 hours after the surgery.
- Secondary Outcome Measures
Name Time Method the total amount of drugs infused for postoperative pain control