Dental Diseases
Conditions
Interventions
Ciprofol Group:During the anesthesia induction phase, a nitrous oxide-oxygen mixture was administered via facemask, and inhaled anesthesia induction was performed using a low-concentration, gradually
Propofol Group (Control Group):During the anesthesia induction phase,a nitrous oxide/oxygen mixture was inhaled via facemask, and inhaled anesthesia induction was performed using a low-concentration,
Sponsors
School of Stomatology , The Fourth Military Medical University
Eligibility
Sex/Gender
All
Age
3 Years to 7 Years
Inclusion criteria
Inclusion criteria: 1. Aged 3 to 7 years. 2. American Society of Anesthesiologists (ASA) physical status I-II. 3. Scheduled for elective dental caries treatment under general anesthesia. 4. Guardians have provided written informed consent.
Exclusion criteria
Exclusion criteria: 1) Upper respiratory tract infection. 2) Cognitive impairment or neurodevelopmental disorders. 3) Congenital diseases. 4) Known allergy to anesthetic agents. 5) Contraindications to ciprofol or propofol. 6) Severe hepatic or renal dysfunction. 7) Congenital craniofacial malformations predisposing to difficult airway.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pediatric Anesthesia Emergence Delirium Scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Emergence Time;Extubation Time;Hemodynamic Stability;Safety of Deep Anesthesia Extubation;Postoperative Pain;postoperative nausea and vomiting(PONV) ; | — |
Countries
China
Contacts
Public ContactZhangYaqiu
School of Stomatology , The Fourth Military Medical University
Outcome results
None listed