RecruitingNot ApplicableNCT07050212

Application of Remimazolam, Dexmedetomidine, and Esketamine in Pediatric Preoperative Sedation

A Comparative Study of the Application of Remimazolam, Dexmedetomidine, and Esketamine in Pediatric Preoperative Sedation


Sponsor

Maternal and Child Health Hospital of Hubei Province

Enrollment

150 participants

Start Date

Apr 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

By comparing the application effects of three drugs in pediatric preoperative sedation, this study explores the optimal medication regimen, aiming to provide safer, more effective, and more personalized medication options for pediatric preoperative sedation. Additionally, this research will also focus on the impact of these three drugs on postoperative agitation in children, offering valuable references for the overall management of pediatric surgical anesthesia.


Eligibility

Min Age: 2 YearsMax Age: 5 Years

Inclusion Criteria3

  • Children aged 2 to 5 years old
  • the American Society of Anesthesiologists (ASA) physical status of Class I
  • scheduled for adenotonsillectomy under general anesthesia, will be included.

Exclusion Criteria4

  • Abnormal lung function and respiratory system function
  • airway obstruction or deformity, history of mental illness
  • electrocardiogram indicating bradycardia
  • history of cardiac disease

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Interventions

DRUGremimazolam group

remimazolam is administered intravenously at a dose of 0.3 mg/kg

DRUGdexmedetomidine group

dexmedetomidine is administered intravenously at a dose of 1 μg/kg

DRUGesketamine group

esketamine is administered intravenously at a dose of 0.5 mg/kg


Locations(1)

Maternal and Child Health Hospital of Hubei Province

Wuhan, Hubei, China

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NCT07050212


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