emergence agitation
Conditions
Interventions
control group:blank control
experimental group 1:S-ketamine was administered 5min before the end of surgery
experimental group 2:Propofol was administered 5 minutes before the end of surgery
Sponsors
Department of Anesthesiology of Xuzhou Children's Hospital, Xuzhou Medical University
Eligibility
Sex/Gender
All
Age
3 Years to 7 Years
Inclusion criteria
Inclusion criteria: 1. Children with tonsillectomy and/or adenoidectomy under elective general anesthesia; 2. Aged from 3 to 7 years; 3. Weight 12-40kg; 4. ASA I-II.
Exclusion criteria
Exclusion criteria: 1. Allergic to S-ketamine or propofol injection; 2. Preoperative hepatic or renal insufficiency or heart disease; 3. Symptoms of upper respiratory tract infection within 1 week before surgery; 4. Children with neurological diseases; 5. The operation time was less than 10min or more than 40min.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of emergence agitation; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative FLACC pain score of the children; | — |
Countries
China
Contacts
Public ContactWu Xiaole
Xuzhou Children's Hospital, Xuzhou Medical University
Outcome results
None listed