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Comparison of VentiBroncTM Anchor With Conventional Double-lumen Endobronchial Tube in Patients With High Risk of Malposition

Endotracheal Intubation Clinical Trial

Official title:
Comparison of VentiBroncTM Anchor With Conventional Double-lumen Endobronchial Tube in Patients With High Risk of Malposition

Clinical Trial Summary

The investigators intend to compare the group using triple-cuffed endobronchial tube (VentiBroncTM Anchor) with the group using the conventional double-lumen endotracheal tube (Shiley®) in patients at high risk of malposition of the double-lumen endotracheal tube. The aim of this study is to determine if the use of VentiBroncTM Anchor increases the success rate of optimal double-lumen intubation to left main bronchus.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06061055
Study type Interventional
Source Yonsei University
Contact Kyuho Lee
Phone 82-02-2224-1636
Email theoneimlee@yuhs.ac
Status Recruiting
Phase N/A
Start date August 14, 2023
Completion date August 2024
View Details
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