NCT03214497

Protector™ Versus Supreme® Laryngeal Mask Airway

Prospective Randomised Trial of the Protector™ Versus the Supreme® Laryngeal Mask Airway

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 96 (actual)
• Sponsor: Schulthess Klinik · Academic / Other
• Sex: All
• Age: 18 Years – 75 Years
• Healthy volunteers: Not accepted

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.

Detailed 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.

Conditions

• Anesthesia

Interventions

Type	Name	Description
DEVICE	Protector	All patients which are assigned to the Protector are studied with this laryngeal mask
DEVICE	Supreme	All patients which are assigned to the Supreme are studied with this laryngeal mask

Timeline

• Start date: 2017-07-12
• Primary completion: 2017-11-28
• Completion: 2017-11-28
• First posted: 2017-07-11
• Last updated: 2017-12-02

Locations

1 site across 1 country: Switzerland