A randomized clinical trial of Arginaid and Arginaid Water as preoperative oral rehydration for the pediatric patients undergoing elective surgery.

A randomized clinical trial of Arginaid and Arginaid Water as preoperative oral rehydration for the pediatric patients undergoing elective surgery. - Arginaid and Arginaid Water as preoperative oral rehydration for the pediatric patients.

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000012376

Enrollment

150

Registered

2013-11-21

Start date

2013-10-29

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric patients undergoing elective surgery

Interventions

Participated patients will be randomly divided into three groups. One is Arginaid Water group, another is Arginaid group the other is clear water group. Patients in Arginaid Wtare group intake Arginai

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Pediatric patients who are scheduled to have elective operations. American Society of Anesthesiologists physical status classification 1or2. Pediatric patients who have submitted a written informed consent.

Exclusion criteria

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.

Design outcomes

Primary

Measure	Time frame
Volume and pH of gastric content just after the induction of general anesthesia	—

Secondary

Measure	Time frame
Hunger and thirst before operations, Adverse events, Taste of the preoperative oral rehydrations	—

Countries

Japan

Contacts

Public ContactYoshikazu Miyamoto

Osaka University graduate school of medicine Department of anesthesiology and intensive care

miyamoto@anes.med.osaka-u.ac.jp+81-6-6879-3133

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026