Identification of risk factors for post-operative nausea and vomiting
Not Applicable
- Conditions
- All surgical patients receiving general anesthesia
- Registration Number
- JPRN-UMIN000052565
- Lead Sponsor
- Chiba University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 1200
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who apply for the following criteria 1) those planned for continued sedation in the intensive care unit 2) those with allergic reaction to either anti-emetics 3) those under steroid treatment pre-operatively planned for steroid cover during anesthesia 4) those determined not-applicable by the responsible personnel
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method PONV score within 24hours post-surgery (0:none~4:vomiting)
- Secondary Outcome Measures
Name Time Method 1) number of vomit within 24 hours post-surgery 2) number of anti-emetics used within 24 hours post-surgery 3) first time meal after surgery and amount of intake