Child Clinical Trial
Official title:
Comparative Study on the Effects of Capacities of Midazolam on Delirium After Sevoflurane Anesthesia in Pediatric Strabismus Surgery : a Randomized Double- Blinded Trial
Sevoflurane with its rapid induction and emergence, hemodynamic stability, and nonirritating
airway properties, has acquired widespread acceptance in children. However, sevoflurane has
been reported to be associated with emergence agitation in children, with a reported
incidence of up to 80%.
The purpose of this study is to verify that the prophylactic use of midazolam, which is a
GABA A receptor inhibitor, given five minutes before the end of strabismus surgery reduces
the incidence of emergence agitation after sevoflurane anesthesia in children.
Simultaneously, this study aims to find out the proper dose of midazolam with minimum
disturbance to patient's emergence time.
Sevoflurane is associated with a high incidence of emergence agitation in children. The etiology of emergence agitation is unclear. Some studies proposed that emergence agitation was related to a variable rate of neurologic recovery rate in different brain areas and immaturity of neurons. Inhalation anesthetics have been known to exert transient paradoxical excitatory effects in both animals and human patients, especially in children. The gamma(γ)-aminobutyric acid (GABA)A receptor is the target depressant effect site of most anesthetic drugs including sevoflurane. Midazolam acts on the benzodiazepine binding site of GABAA receptors and results in inhibitory effects on the central nervous system. The effect of midazolam premedication, as well as midazolam administration at the end of surgery, on suppressing emergence agitation has been studied. However, the effect of midazolam on emergence agitation is still controversial. This study aims to figure out the effect of midazolam at the end of surgery on emergence agitation during the recovery period, and find out the proper dose of midazolam with minimum disturbance to patient's emergence time. ;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention
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