Protector™ Versus Supreme® Laryngeal Mask Airway

Status Completed

Clinical Trial Summary

The goal of this study is to compare the oropharyngeal leak pressure of the Protector Laryngeal mask with the Supreme laryngeal mask. Other secondary parameters will be studied.

Clinical Trial Description

The OLP as the primary outcome measurement will be evaluated after insertion of the LMA in each group. We hypothesize that there will be a difference of 4 cm H2O between the 2 masks, because of the different material and slightly different form of the masks. Secondary outcomes will be measured after insertion of the LMA as by protocol. Finally postoperative airway morbidity will be evaluated 3 hours after removal of the LMA. ;

Study Design

Related Conditions & MeSH terms

Anesthesia

Clinical Trial Details

NCT number	NCT03214497
Study type	Interventional
Source	Schulthess Klinik
Contact
Status	Completed
Phase	N/A
Start date	July 12, 2017
Completion date	November 28, 2017

View Details

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