At a glance
ClinicalIndex Comparison RecordN/ACompleted· 94 enrolled
Drug / intervention
AuraGain +1 moredevice
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.
A Randomized Comparison of Ambu AuraGain (Original Name of Product) Laryngeal Mask Airway and I-gel in Children
In Brief
A clinical study evaluating AuraGain and I-gel for General Anesthesia. Completed, enrolled 94 participants across 1 site.
Detailed Summary
Children aged below 7 years are randomly assigned to AuraGain Group or I-gel group. After anesthetic induction, AuraGain or I-gel is inserted and mechanical ventilation is started. Oropharyngeal leak pressure, peak inspiratory pressure, success rate for insertion, ease for insertion, ease for gastric tube insertion and fiberoptic bronchoscopic views will be compared between two groups.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsGeneral Anesthesia
CountriesSouth Korea
Collaborators--
Timeline
N/ACompletedFinished
201820192020202120222023202420252026
First PostedApr 2017
Enrollment StartJun 2017
Primary CompletionMay 2018
TodayJul 2026
First PostedApr 18, 2017
Enrollment StartJun 12, 2017
Primary CompletionMay 31, 2018
TodayJul 1, 2026
Enrollment to primary: 12 monthsPosted 9.2 years ago
Interventions
AuraGaindevice
After anesthetic induction, AuraGain is inserted in children
I-geldevice
After anesthetic induction, I-gel is inserted in children