The time-dependent change of leak pressure of i-gel in childre
Not Applicable
Recruiting
- Conditions
- pediatric patients considered suitable for general anesthesia with i-gel
- Registration Number
- JPRN-UMIN000013024
- Lead Sponsor
- Department of Anesthesiology, Sapporo Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 36
Inclusion Criteria
Not provided
Exclusion Criteria
emergent surgery, patients with high risk of aspiration, patients with difficult airway, patients with congenital deformation of airway, patients with cervical spine disease, patients with symptom of airway infection, patients with sever respiratory/cardiovascular disease
Study & Design
- Study Type
- Observational
- 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 molecular mechanisms influence i-gel leak pressure changes in pediatric anesthesia?
How does i-gel leak pressure compare to standard airway devices in pediatric patients over time?
Are there specific biomarkers that correlate with i-gel performance in children under general anesthesia?
What adverse events are associated with prolonged i-gel use in pediatric anesthesia and how are they managed?
What alternative airway management strategies or devices are being studied for pediatric patients with similar indications?