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A Comparative Study of the 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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116741
Enrollment
Unknown
Registered
2026-01-14
Start date
2025-03-19
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Pediatric Preoperative Separation Anxiety

Interventions

Remimazolam Group:Before entering the operating room, an intravenous access is established. Under the accompaniment of a parent, remimazolam is administered intravenously at a dose of 0.3 mg/kg, with
Esketamine Group:Before entering the operating room, an intravenous access is established. Under the accompaniment of a parent, esketamine is administered intravenously at a dose of 0.5 mg/kg, with co
Dexmedetomidine Group:Before entering the operating room, an intravenous access is established. Under the accompaniment of a parent, dexmedetomidine is administered intravenously at a dose of 1 µg/kg,

Sponsors

Hubei Maternal and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 5 Years

Inclusion criteria

Inclusion criteria: Children aged 2 to 5 years old with an American Society of Anesthesiologists (ASA) physical status of Class I, who are scheduled for adenotonsillectomy under general anesthesia, will be included.

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Sedation success rate;Onset time of sedation;Parent-Child Separation Anxiety Score (PASA Score);Heart rate, blood pressure, respiratory rate, and pulse oximetry saturation at 0, 3, 5, and 10 minutes after administration of the sedative.;Recovery time;

Secondary

MeasureTime frame
Mask Acceptance Score (MAS);ncidence of adverse reactions during intravenous bolus administration of sedative drugs and anesthesia induction;

Countries

China

Contacts

Public ContactJin Shuangfen

Hubei Maternal and Child Health Hospital

553684828@qq.com+86 182 7147 0350

Outcome results

None listed

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