Comparison of laryngeal mask insertion in pediatric airway management
Not Applicable
- Conditions
- Inguinal hernia.Inguinal hernia
- Registration Number
- IRCT20170516033992N3
- Lead Sponsor
- Oroumia University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 68
Inclusion Criteria
elective herniorrhaphy candidates with ASA1 and ASA2
Given permission to participate in the study
Exclusion Criteria
ASA3 and higher patients
patients who require urgent surgery required with the risk of aspiration from the stomach fluids
patients with full stomach and therefore with higher risk of aspiration of fluids
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Chest movement. Timepoint: Through anesthesia procedure in the operation room. Method of measurement: Observation (No movement, Partially good, Adequately good).;Airway pressure. Timepoint: Through anesthesia procedure in the operation room. Method of measurement: Adjustable Pressure Limiting results.;Time of Laryngeal mask insertion. Timepoint: Through anesthesia procedure in the operation room. Method of measurement: Clock.;Mucous damage. Timepoint: After extracting the mask. Method of measurement: presence of blood on the mask.;Times tried to put the laryngeal mask on. Timepoint: In time of getting the mask. Method of measurement: Observation.
- Secondary Outcome Measures
Name Time Method Chest movement. Timepoint: Through anesthesia procedure in the operation room. Method of measurement: Observation (no movement, partially good, adequately enough).