Comparison of Propofol 1mg/kg and Propofol 0.5mg/kg for Prevention of Emergence Agitation in Children Undergoing Strabismus Surgery During Sevoflurane Anesthesia
Strabismus
About this trial
This is an interventional prevention trial for Strabismus focused on measuring emergence agitation, propofol, strabismus surgery, children, elective strabismus surgery
Eligibility Criteria
Inclusion Criteria:
- children (3-12 years old) scheduled for elective strabismus surgery undergoing general anesthesia.
- ASA 1-2
Exclusion Criteria:
1. Patients with developmental disability, mental retardation, neurologic disorder, ongoing neurologic medication such as anticonvulsant, previously undergoing general anesthesia, a recent history of upper respiratory infection, parents difficult to read or understand the informed consent.
Sites / Locations
- Gangnam Severance Hospital, Yonsei University College of MedicineRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Placebo Comparator
1) propofol 1.0mg/kg group
2) propofol 0.5mg/kg group
3) normal saline group
According to randomly allocated group, propofol 1.0mg/kg, propofol 0.5mg/kg or normal saline will be intravenously administered at the end of surgery
According to randomly allocated group, propofol 1.0mg/kg, propofol 0.5mg/kg or normal saline will be intravenously administered at the end of surgery
According to randomly allocated group, propofol 1.0mg/kg, propofol 0.5mg/kg or normal saline will be intravenously administered at the end of surgery