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

NCT01575236 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2012-08-08

No results posted yet for this study

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.

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

Sponsors & Collaborators

  • Medical University Innsbruck

    collaborator OTHER

  • Schulthess Klinik

    lead OTHER

Principal Investigators

  • Christian Keller, MD MSc · Anästhesie Schulthess Klinik

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-03-31
Primary Completion
2012-06-30
Completion
2012-07-31

Countries

  • Austria

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01575236 on ClinicalTrials.gov