Comparing the efficacy of two different types of airway devices in children undergoing surgery.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)ASA I and II patients.
2)Both male and female patients between 1-12 years of age.
3)Elective procedures under General Anaesthesia.
Exclusion Criteria
1.Parents/Patients attendant not giving consent.
2.Weight less than 5 kg.
3.Patients with BMI > 30 kg/m2.
4.History of recent upper respiratory tract infection.
5.Inadequate fasting.
6.Patients with contraindications to SAD (restricted mouth opening, upper airway obstruction etc.).
7.Patients with abnormal/distorted anatomy of the upper airway.
8.Head, neck and oral surgery.
9.Patients with increased risk of aspiration (GERD, Hiatus Hernia etc.).
10.Emergency surgeries.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Oropharyngeal Leak Pressure will be measured as the primary outcome.Timepoint: Immediately after supraglottic airway device insertion.
- Secondary Outcome Measures
Name Time Method