Expired Study
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Chicago, Illinois 60618


Purpose:

The purpose of this study is to compare the clinical efficacy of the air-Q ILA-SP with the current standard of care, the LMA Unique in anesthetized non-paralyzed pediatric patients.


Study summary:

The goal for this randomized, non-crossover investigation is to compare a disposable version of the standard LMA, LMA Unique TM,with the air-Q ILA-SP in pediatric patients. Oropharyngeal leak pressure is commonly used as an indicator of airway seal adequacy. Similarly, flexible fiberoptic bronchoscope examination is often employed to assess proper placement of airway devices. We hypothesize that airway leak pressures with the ILA-SP will be superior to the LMA upon initial device placement, and ten minutes after device placement. Airway leak pressures will be measured by recording the circuit pressure at which equilibrium is reached. Ease of placement, fiberoptic grade of laryngeal view, and complications (airway related, gastric insufflation, trauma) will also be assessed.


Criteria:

Inclusion Criteria: - Children undergoing general anesthesia using a supraglottic airway device - 3 to 9 years of age - 20 to 30 kilograms in weight Exclusion Criteria: - History of a difficult airway - Active gastrointestinal reflux - Active upper respiratory tract infection


NCT ID:

NCT01385761


Primary Contact:

Principal Investigator
Narasimhan Jagannathan, MD
Childrens Memorial Hospital


Backup Contact:

N/A


Location Contact:

Chicago, Illinois 60618
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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