Randomized clinical trial comparing the quality of recovery among overnight fasting, preoperative oral rehydration solution, and preoperative oral carbohydrate
Not Applicable
- Conditions
- Patients scheduled for the surgery of body surface
- Registration Number
- JPRN-UMIN000009388
- Lead Sponsor
- Department of Anesthesiology, Yokohama City University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with impaired gastrointestinal motility, gastroesophageal reflux, potential difficult airway, poor Japanese comprehension, or psychiatric disturbance
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Quality of recovery, 24 hours after anesthesia
- Secondary Outcome Measures
Name Time Method