Preventive effect of postoperative nausea and vomiting will be correlated with the dose of intraoperative acetaminophen : a randomized clinical trial about patients without pai
Not Applicable
- Conditions
- Orthopedic upper limb or leg disorders
- Registration Number
- JPRN-UMIN000031457
- Lead Sponsor
- Department of anesthesiology,National hospital organization Saitama hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 180
Inclusion Criteria
Not provided
Exclusion Criteria
patients with liver or kidney disfunction or dementia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative nausea and vomiting evaluation performed by numerical rating scale(NRS) after 30 minutes,2 hours,6 hours,24 hours postoperatively.
- Secondary Outcome Measures
Name Time Method