A randomized clinical trial of Arginaid and Arginaid Water as preoperative oral rehydration for the pediatric patients undergoing elective surgery.
Not Applicable
Recruiting
- Conditions
- Pediatric patients undergoing elective surgery
- Registration Number
- JPRN-UMIN000012376
- Lead Sponsor
- Osaka University graduate school of medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
Not provided
Exclusion Criteria
Obstruction of upper gastrointestinal tract, Ileus, dysphasia, Severe obesity (Body Mass Index>35), Increased intracranial pressure, recurrent nerve paralysis, Patients who are predicted to have difficulties in tracheal intubation, Patients who need pre-medications, A serum phosphorus>6mg/dL, Decision as ineligible by principal investigators.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Volume and pH of gastric content just after the induction of general anesthesia
- Secondary Outcome Measures
Name Time Method Hunger and thirst before operations, Adverse events, Taste of the preoperative oral rehydrations