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

PHASE3CompletedINTERVENTIONAL
Enrollment

120

Participants

Timeline

Start Date

March 31, 2012

Primary Completion Date

June 30, 2012

Study Completion Date

July 31, 2012

Conditions
Adverse Anesthesia Outcome
Interventions
DEVICE

Guardian Laryngeal Mask

ease of insertion, oropharyngeal seal pressure, fiberoptic position, ease of ventilation, occult blood, gastric insertion

DEVICE

Supreme Laryngeal Mask Airway

ease of insertion, oropharyngeal seal pressure, fiberoptic position, ease of ventilation, occult blood, gastric insertion

Trial Locations (1)

6020

Universitätsklinik für Anästhesie, Innsbruck

All Listed Sponsors
collaborator

Medical University Innsbruck

OTHER

lead

Schulthess Klinik

OTHER

NCT01575236 - A Randomized Non Crossover Study of the GuardianTM Versus SupremeTM Laryngeal Mask Airway | Biotech Hunter | Biotech Hunter