Gastric Insufflation Volume Using I-gel Versus Ambu AuraGain in Pediatric Patients Undergoing Elective Orthopedic Operations Under General Anesthesia

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age2-12
SponsorTanta University

About this trial

Our study aimed to compare the gastric insufflation volume between Ambu AuraGain and i-gel and its relationship with the oropharyngeal sealing pressure and the incidence of postoperative complications in generally anesthetized controlled-ventilated pediatric patients undergoing elective orthopedic operations.

Eligibility criteria

Qualifiers

Aged from 2 to 12 years.

Both sexes.

American Society of Anesthesiologists (ASA) physical status I and II.

Scheduled for elective orthopedic operations in a supine position under general anesthesia.

Disqualifiers

Patients with a known history of gastro-oesophageal reflux disorders.

Full Stomach.

Anticipated difficult mask ventilation or intubation.

Body mass index "BMI" exceeding 20% of the ideal.

Trial design

Treatments tested in this trial

  • Ambu Auragain
  • I-gel

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators