At a glance
ClinicalIndex Comparison RecordN/ACompleted· 54 enrolled
Drug / intervention
Propofoldrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
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
In Brief
A clinical study evaluating Propofol for Pediatric ALL. Completed, enrolled 54 participants across 1 site.
Detailed 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
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPediatric ALL
CountriesIndonesia
Collaborators--
Timeline
N/ACompletedFinished
20192020202120222023202420252026
First PostedMay 2018
Enrollment StartMay 2018
Primary CompletionAug 2018
TodayJul 2026
First PostedMay 18, 2018
Enrollment StartMay 31, 2018
Primary CompletionAug 31, 2018
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 8.1 years ago
Interventions
Propofoldrug
Those who received intravenous propofol