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GMA-TulipTM, i-gelTM and the LMA-SupremeTM (LMA-S) Devices in Airway Management

Anesthesia Clinical Trial

Official title:
GMA-TulipTM, i-gelTM and the LMA-SupremeTM (LMA-S) Devices in Airway Management Under General Anesthesia, a Randomized Controlled Study

Clinical Trial Summary

Patients were randomly assigned to three extraglottic airway (EGA) devices groups for airway management after anesthesia induced. Fiberoptic bronchoscope (FB) guided glottic exposure grading was performed and other airway management quality was recorded.

Clinical Trial Description

Mechanical ventilation was volume controlled and time cycled with tidal volumes (6-8 ml/kg) set to maintain peak inspiratory pressures of less than 20 cm H2O and ventilatory frequency adjusted to maintain end-tidal carbon dioxide (PETCO2) at 35-45 mmHg. Then a fiberoptic bronchoscope was passed through airway tube into the device to perform glottic exposure grading. Peak airway pressure, incidence of pharyngalgia, bleeding, hoarseness, and dysphagia were recorded. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06383494
Study type Interventional
Source Zhejiang Cancer Hospital
Contact Jiangling Wang, Ph.D
Phone +86 571 88122106
Email wangjl@zjcc.org.cn
Status Recruiting
Phase N/A
Start date April 30, 2024
Completion date December 30, 2025
View Details
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