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The safety and feasibility of early postoperative oral syrup comsumption after general anesthesia in pediatric patients: A prospective randomized controlled trial

The safety and feasibility of early postoperative oral syrup comsumption after general anesthesia in pediatric patients: A prospective randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16008197
Enrollment
Unknown
Registered
2016-03-31
Start date
2016-04-01
Completion date
Unknown
Last updated
2019-12-16

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

Conditions

Children accepted surgery and general anesthesia

Interventions

early oral hydration group (EOH):early postoperative oral syrup comsumption after general anesthesia in pediatric patients
Control:water deprivation

Sponsors

PACU, West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 14 Years

Inclusion criteria

Inclusion criteria: Nonesophagectomy and Nongastrointestinal surgery, ASA physical score 1 to 3, good mental status,cough an swallowing reflex retum normal, myodynamia of four limbs: level V,last dose of analgesic has been given for more than twenty minutes.

Exclusion criteria

Exclusion criteria: upper respiratory infection, facial surgery, pharyngeal or laryngeal surgery,difficulty swallowing, nausea and vomiting, abdominal operation were excluded.

Design outcomes

Primary

MeasureTime frame
nausea;vomiting;thirsty scale;—

Secondary

MeasureTime frame
satisfaction scale;oropharyngeal discomfort scale;drink desire;—

Countries

China

Contacts

Public ContactXiao-rong Yin

PACU, West China Hospital, Sichuan University

1813864144@qq.com+86 18980601570

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 26, 2026