Clinical Trials Directory

Trials / Completed

CompletedNCT02820792

Non-Crossover Study of the LMA Protector Versus Ambu AuraGain

A Randomized Non-Crossover Study of the LMA ProtectorTM Versus Ambu Aura GainTM in Adult Patients

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
96 (actual)
Sponsor
Schulthess Klinik · Academic / Other
Sex
All
Age
19 Years – 65 Years
Healthy volunteers
Not accepted

Summary

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

Conditions

Interventions

TypeNameDescription
PROCEDUREfunction testsfunction tests: ease of insertion, oropharyngeal seal pressure, fiberoptic position, ease of ventilation, occult blood, gastric tube insertion
DEVICELMA ProtectorTM
DEVICEAmbu AuraGainTM

Timeline

Start date
2016-09-01
Primary completion
2016-12-01
Completion
2016-12-20
First posted
2016-07-01
Last updated
2017-01-26

Locations

2 sites across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT02820792. Inclusion in this directory is not an endorsement.