Comparative Evaluation of Periglottic Airway Devices With Performed Shape

Status Recruiting

Clinical Trial Summary

The purpose of this study is to evaluate four, most popular periglottic airway devices as regards to ventilation sufficiency and perfection of installation/ anatomical application to the larynx (evaluation with fiberscope).

Clinical Trial Description

After being informed about the study and potential risks, all patients (>18 years old scheduled for elective surgery under general anesthesia) giving written informed consent will undergo preoperative screening examination to determine eligibility for study entry. A randomization process has been previously done, according to which the participants have been classified into one of the four groups of the study. Each study group is scheduled to receive one of the four periglottic devices (LM FastrachTM, LM ProsealTM, LM I-GelTM, LM ProtectorTM) while evaluating the ventilation sufficiency and perfection of installation/ anatomical application to the larynx (evaluation with fiberscope). ;

Study Design

Related Conditions & MeSH terms

Airway Management

Clinical Trial Details

NCT number	NCT05639439
Study type	Interventional
Source	University Hospital of Patras
Contact	Maria Spyraki, MD, MSc
Phone	00306944471259
Email	maria.uop@gmail.com
Status	Recruiting
Phase	N/A
Start date	April 1, 2021
Completion date	April 30, 2024

View Details

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