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Effect of low-dose Esketamine versus propofol on emergence agitation during awakening in children with daytime ophthalmology: a randomized single-blind controlled trial

Effect of low-dose Esketamine versus propofol on emergence agitation during awakening in children with daytime ophthalmology: a randomized single-blind controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072431
Enrollment
Unknown
Registered
2023-06-13
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-06-18

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

Conditions

emergence agitation

Interventions

Esketamine group:0.3mg/kg esketamine
Propofol group:1mg/kg propofo

Sponsors

Guangzhou Women and Children’s Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 7 Years

Inclusion criteria

Inclusion criteria: 1. The legal guardian of the child signs the informed consent 2. Ophthalmic day surgery (meibomian gland cyst, trichiasis, strabismus) 3. Monocular surgery 4.ASA Grade I-II 5. Ages 3-7

Exclusion criteria

Exclusion criteria: 1. Allergy to drugs used in this study 2. There are contraindications for the use of this drug 3. You have mental illness 4. The child or the legal guardian of the child withdrew from the experiment or refused to cooperate with the data collection

Design outcomes

Primary

MeasureTime frame
emergence agitation;—

Secondary

MeasureTime frame
Recovery time (minutes);Extubation time (minutes);PACU residence time (minutes);Number of cases of EA treated with propofol addition during recovery period;—

Countries

China

Contacts

Public ContactNa Zhang

Guangzhou Women and Children’s Medical Center

na999666@163.com+86 135 6040 9867

Outcome results

None listed

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