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A Randomized Non Crossover Study of the GuardianTM Versus SupremeTM Laryngeal Mask Airway

Adverse Anesthesia Outcome Clinical Trial

Official title:
A Randomized Non Crossover Study of the GuardianTM Versus SupremeTM Laryngeal Mask Airway

Clinical Trial Summary

The investigators test the hypothesis that ease of insertion, oropharyngeal leak pressure, fiberoptic position and ease of gastric tube placement differ between the GuardianTM and the LMA SupremeTM in paralyzed, anesthetized patients.

Clinical Trial Description

The GuardianTM is a new extraglottic airway device which brings together features of both the LMA ProSealTM (high seal cuff, gastric access and bite block - to facilitate ventilation, airway protection and airway obstruction, respectively) and the LMA UniqueTM (single use - prevention of disease transmission). In the following randomized, non-crossover study, the investigators test the hypothesis that ease of insertion, oropharyngeal leak pressure, fiberoptic position and ease of gastric tube placement differ between the GuardianTM and the LMA SupremeTM in paralyzed, anesthetized patients. ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01575236
Study type Interventional
Source Schulthess Klinik
Contact
Status Completed
Phase Phase 3
Start date March 2012
Completion date July 2012
View Details
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