Emergence agitation
Conditions
Interventions
Group P:Propofol, intravenous injection (1-2mg/kg)
Group D:Dexmedetomidine, intravenous injection (0.5-1ug/kg)
Sponsors
Children's Hospital of Soochow University
Eligibility
Sex/Gender
All
Age
1 Years to 14 Years
Inclusion criteria
Inclusion criteria: 1. Children who undergo elective surgery and have agitation during the resuscitation period; 2. American Society of Anesthesiologists (ASA) score I or II; 3. Aged 1-14 years, male or female; 4. Sign the informed consent.
Exclusion criteria
Exclusion criteria: 1. History of upper respiratory tract infection within 2 weeks before surgery; 2. A history of heart disease and mental illness; 3. A history of allergy to dexmedetomidine, propofol or other narcotic drugs; 4. A history of neurological and neuromuscular diseases; 5. Liver and kidney dysfunction; 6. Maxillofacial deformity or abnormal development.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pediatric Anesthesia Emergence Delirium (PAED); | — |
Secondary
| Measure | Time frame |
|---|---|
| Time in the resuscitation room; | — |
Countries
China
Contacts
Public ContactXuemin Han
Children's Hospital of Soochow University
Outcome results
None listed