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The depth of anesthesia and emergence agitation in children for day-surgery

A single-center, observational cohort study for the depth of anesthesia and emergence agitation (EA) / emergence delirium (ED) in children for day-surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200062680
Enrollment
Unknown
Registered
2022-08-15
Start date
2022-09-01
Completion date
Unknown
Last updated
2023-04-12

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

Conditions

Postoperative emergence agitation

Interventions

General anesthesia:None

Sponsors

Affiliated Hospital of Zunyi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Children aged 4-12 years undergoing general anesthesia day-surgery; 2. American Society of Anesthesiologists physical status I or II.

Exclusion criteria

Exclusion criteria: 1. Children with obstructive sleep apnea syndrome, any developmental delays, psychological disorder, mental or neurological disorders; 2. Children has a history of allergic or adverse reaction to medications required by the study protocol; 3. Children take medicine affecting the central nervous system before surgery; 4. Children undergoing heart and brain surgery; 5. Sedative infusion (less than 24h before the study) including propofol, morphine, fentanyl, midazolam, ketamine, and dexmedetomidine.

Design outcomes

Primary

MeasureTime frame
Risk factors for postoperative emergence agitation (EA) / emergence delirium (ED);—

Secondary

MeasureTime frame
Relationship between the depth of anesthesia and emergence agitation (EA) / emergence delirium (ED);—

Countries

China

Contacts

Public ContactZhang Yinan

Affiliated Hospital of Zunyi Medical University

zynluoyang@163.com+86 13908523226

Outcome results

None listed

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