Propofol to Reduce the Incidence of Postanesthetic Emergence Agitation in Pediatric Patients Under General Anesthesia

• Status: Completed
• Trial end date: 2018-08-31
• Target enrollment: 0
• Participant gender: All

Summary

This study aimed to know the effectivity of 0.5 mg/kg propofol in the end of anesthesia to reduce the incidence of postanesthetic emergence agitation in pediatric patients under general inhalation anesthesia

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Indonesia University
• Treatments: Anesthetics; Propofol

Criteria

Inclusion Criteria:

• Patient undergoing non-emergency surgery with general anesthesia

• Patient using sevoflurane as anesthetic agent

• Patient aged 1 - 5 years old

• American Society of Anesthesiologists (ASA) physical status 1 - 2

• Patient family signed the informed consent to be included in the study

Exclusion Criteria:

• Patient that will undergo ophthalmologic and otorhinolaryngologic surgery

• Patient that will require post operation stay in Intensive Care Unit

• Patient with psychological and neurological problem

• Patient with developmental delay

• Patient using sedative drugs

• Patient with allergy to propofol

• Patient or patient family with history of malignant hyperthermia

• Patient with difficulty on intubation and ventilation

• Patient with cardiovascular disease

• Patient with hemodynamic instability