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Comparison of Size 1 I-gel and ProSeal Laryngeal Mask

NCT01704118 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2012-10-11

No results posted yet for this study

Summary

Objective of this prospective, randomized and controlled study is to compare the performances of recently-released size 1 I-gel and size 1 PLMA proven to be superior to classical LMA with prospective studies. In this study, primer endpoint was value of airway leak pressure and secondary insertion time, insertion success and conditions, initial airway quality, hemodynamic parameters, fiberoptic view and complications will be assessed.

Conditions

  • Laryngeal Masks

Interventions

DEVICE

I-gel

Supraglottic airway device

DEVICE

ProSeal Laryngeal mask

Supraglottic airway device

Sponsors & Collaborators

  • Inonu University

    lead OTHER

Principal Investigators

  • Gulay Erdogan Kayhan · Assistant Professor, MD

Study Design

Allocation
RANDOMIZED
Masking
SINGLE
Model
PARALLEL

Eligibility

Max Age
6 Months
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-01-31
Primary Completion
2012-09-30
Completion
2012-10-31

Countries

  • Turkey (Türkiye)

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 NCT01704118 on ClinicalTrials.gov