Study of effectiveness of acetaminophen for the postoperative pain after total hip arthroplasty
Not Applicable
- Conditions
- hip osteoarthritis
- Registration Number
- JPRN-UMIN000022778
- Lead Sponsor
- Hyogo colleage of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
Patients have a liver function disorder, a renal function disorder. In disease severity of the liver function, we exclude the cases more than grade 2 or class B from the object of this study with "pharmaceutical products side effect serious degree classification" "Child-Pugh classification". In disease severity of the renal function, we excluded the case of Ccr<59. Cases with a history of the past of hypersensitivity. The cases that has difficulty in mutual understanding in self.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pre-operative assessment Numerical Rating Scale (NRS) value. Post-operative assessment NRS (0 hour, 6 hours, 12 hours, 18 hours, 24 hours, 36 hours, 48 hours)
- Secondary Outcome Measures
Name Time Method Patient Controlled Analgesia used amount Opioid consumption volume of 24 hours Postoperative liver function evaluation during 2weeks