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Comparison of the effects of fluid intake 2 and 4 hours after general anesthesia in pediatric ophthalmology and otolaryngology patients

Comparison of the effects of fluid intake 2 and 4 hours after general anesthesia in pediatric ophthalmology and otolaryngology patients; open label,randomized controlled post test only design

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0010659
Enrollment
142
Registered
2025-06-23
Start date
2023-09-22
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

None listed

Interventions

Behavioral : The assignment of the experimental group and the control group was random. The experimental group began drinking water 2 hours after the end of general anesthesia, and the control group

Sponsors

Samsung Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Pediatric patients aged 5 to 12 years who are scheduled to undergo ophthalmology or otolaryngology surgery under general anesthesia. 2) Patients who understand the purpose of this study and agree to participate in the study, whose children consent and whose parents give written consent. 3) American Society of Anesthesiology(ASA) level ?,? 4) Patients who are conscious, able to communicate, and use numeric scored scales 5) Patients who returned to the ward after being assessed a PACU(Post Anesthesia Care Unit) score of 9 or higher in the recovery room.

Exclusion criteria

Exclusion criteria: 1) Patients with symptoms of respiratory infection (cough, runny nose, nasal congestion, sore throat, difficulty breathing) before surgery. 2) Patients who have undergone esophageal surgery, tonsillar cancer surgery, oropharyngeal surgery, laryngeal surgery, thoracic surgery, gastrointestinal surgery, and cranial nervous system surgery. 3) Patients undergoing tests or treatment related to gastroesophageal reflux disease. 4) Patients with esophageal stricture or achalasia 5) Patients with diabetes accompanied by gastric atony. 6) Patients with renal failure. 7) Patients with intestinal disease. 8) Patients with surgical contraindications to postoperative dietary intake.

Design outcomes

Primary

MeasureTime frame
Nausea

Secondary

MeasureTime frame
Thrist;The total number of vomiting episodes;Patient satisfaction

Countries

Korea, Republic of

Contacts

Public ContactBora Park

Samsung Medical Center

aluo@naver.com+82-2-3410-0570

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026