Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07050212

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
Phase
N/A
Study type
Interventional
Enrollment
150 (estimated)
Sponsor
Maternal and Child Health Hospital of Hubei Province · Academic / Other
Sex
All
Age
2 Years – 5 Years
Healthy volunteers
Accepted

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.

Detailed description

Participants will be randomly allocated to three groups: remimazolam group(Group A), dexmedetomidine group(Group B), esketamine group(Group C). Before entering the operating room, an intravenous access is established. Under the accompaniment of a parent, one of the three drugs is administered intravenously.

Conditions

Interventions

TypeNameDescription
DRUGremimazolam groupremimazolam is administered intravenously at a dose of 0.3 mg/kg
DRUGdexmedetomidine groupdexmedetomidine is administered intravenously at a dose of 1 μg/kg
DRUGesketamine groupesketamine is administered intravenously at a dose of 0.5 mg/kg

Timeline

Start date
2025-04-01
Primary completion
2026-03-01
Completion
2026-03-01
First posted
2025-07-03
Last updated
2025-07-10

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07050212. Inclusion in this directory is not an endorsement.