In patients of 2 to 12 years, with laryngeal mask airway device based general anaesthesia, with and without the application of positive end expiratory pressure and calculating leak volume in time intervals of 5 mins, 15 mins, 30 mins, and 1 hour to assess the affectiveness of ventilation.
Phase 3
Not yet recruiting
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/07/070072
- Lead Sponsor
- Dr Sriya V Tallapragada
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age 2 to 12 years of age
ASA l and ll
Elective Surgeries
Consent given
Exclusion Criteria
Airway deformities (congenital)
Risk of aspiration
Preoperative sore throat or upper respiratory tract infection
Allergy to local anaesthetic
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What are the molecular mechanisms of I-gel laryngeal mask airway in pediatric ventilation?
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What adverse events are associated with I-gel use in pediatric general anesthesia?
How does I-gel compare to other airway devices in managing pediatric ventilation leaks?