None
Conditions
Interventions
Group C1:The patient received 0.4mg/kg ciprofol for anesthesia induction and maintenance
Group C2:The patient received 0.4mg/kg ciprofol for anesthesia induction and maintenance
Group P:The patient received 2.0mg/kg propofol for anesthesia induction and maintenance
Sponsors
The First Affiliated Hospital of Guangxi Medical University
Eligibility
Sex/Gender
All
Age
1 Years to 12 Years
Inclusion criteria
Inclusion criteria: 1) ASA?~? grade 2) Children who plan to receive elective tracheoscopy 3) Age range from 1 to 10 years 4) BMI18~28kg/m2.
Exclusion criteria
Exclusion criteria: 1) Patients with a history of anaesthetic drug allergy 2) Congenital heart disease (tetralogy of Fallot, patent ductus arteriosus, ventricular septal defect, pulmonary hypertension) 3) People with severe neurological and mental diseases and cognitive dysfunction 4) Patients with perioperative experience of general anesthesia within 4 weeks.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sedation success rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Injection pain;Blood pressure;Heart rate;SpO2; | — |
Countries
China
Contacts
Public ContactZhong Yu
The First Affiliated Hospital of Guangxi Medical University
Outcome results
None listed