TCTR20150720003CompletedPhase 3
The Comparison of Local infiltration analgesia and Adductor canal block on postoperative pain and Functional outcome after Total knee replacement
Research Affairs Faculty of medicine, Chulalongkorn University0 sites60 target enrollmentStarted: July 20, 2015Last updated:
Conditions
Trial Snapshot
- Phase
- Phase 3
- Status
- Completed
- Sponsor
- Enrollment
- 60
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 Years to 0 N/A (No limit) (—)
- Sex
- All
Inclusion Criteria
- •Patient aged > 18 years old, who was scheduled for total knee arthroplasty
- •American Society of anesthesiologist class 1-3
- •Patient BMI 18-40 kg/m2
Exclusion Criteria
- •refuse to participate this study
- •allergy to any drug in this study
- •age <18 years
- •ASA physical status > 3
- •BMI < 18 kg/m2, BMI > 40 kg/m2
- •contraindication to neuraxial anesthesia
- •uncontrolled hypertension or Blood pressure greater than 140/90 mmmHg
- •history of heart failure, cerebrovascular disease, cardiac surgery, coronary artery disease
- •history of upper GI bleeding, gastric ulcer
- •history of abnormal liver enzyme, hepatic failure, renal failure, organ transplantation, coagulopathy
- •chronic opioids user defined as using opioids drug almost/everyday for three consecutive months or more than 60 mg/day for one month
- •neuropathic pain
- •failure to single shot adductor canal block
- •inability to cooperate with Time Up and Go Test before surgery
Investigators
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