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
| Type | Name | Description |
|---|---|---|
| DRUG | remimazolam group | remimazolam is administered intravenously at a dose of 0.3 mg/kg |
| DRUG | dexmedetomidine group | dexmedetomidine is administered intravenously at a dose of 1 μg/kg |
| DRUG | esketamine group | esketamine 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.