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The i-GelTM. A Randomized, Crossover Study With the Laryngeal Mask Airway ProSealTM in Anesthetized Pediatric Patients

NCT01425151 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2011-09-22

No results posted yet for this study

Summary

In the following randomized, crossover study, the investigators test the hypothesis that ease of insertion and oropharyngeal leak pressure differ between the LMA ProSealTM and the i-GelTM in anesthetized pediatric patients.

Conditions

  • Device Success Rate
  • Device Performance

Interventions

DEVICE

i-Gel

Oropharyngeal leak pressure Insertion success

DEVICE

ProSeal

Oropharyngeal leak pressure Insertion success

Sponsors & Collaborators

  • Schulthess Klinik

    lead OTHER

Principal Investigators

  • Christian Keller, MD, M.Sc. · Schulthess Klinik

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Months
Max Age
6 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2011-09-30
Completion
2011-09-30

Countries

  • Austria
  • Switzerland

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 NCT01425151 on ClinicalTrials.gov