NCT06061055

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

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 154 (actual)
• Sponsor: Yonsei University · Academic / Other
• Sex: All
• Age: 20 Years – 85 Years
• Healthy volunteers: Not accepted

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.

Conditions

• Endotracheal Intubation

Interventions

Type	Name	Description
DEVICE	Intubation with VentiBronc Anchor endobronchial double-lumen tube	Patients in this group are intubated with triple-cuffed double-lumen endobronchial tube (VentiBronc Anchor).
DEVICE	conventional double-lumen intubation	Patients in this group are intubated with conventional double-lumen endobronchial tube (Shiley).

Timeline

• Start date: 2023-10-26
• Primary completion: 2024-11-26
• Completion: 2024-11-26
• First posted: 2023-09-29
• Last updated: 2024-12-12

Locations

1 site across 1 country: South Korea