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

Yonsei University154 enrolled

Overview

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.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

SINGLE

Enrollment

154

Conditions

Endotracheal Intubation

Interventions

Intubation with VentiBronc Anchor endobronchial double-lumen tubeDEVICE

Patients in this group are intubated with triple-cuffed double-lumen endobronchial tube (VentiBronc Anchor).

conventional double-lumen intubationDEVICE

Patients in this group are intubated with conventional double-lumen endobronchial tube (Shiley).

Eligibility

Sex: ALLMin age: 20 YearsMax age: 85 Years

Medical Language ↔ Plain English

Inclusion Criteria: Patients requiring left double-lumen endotracheal tube intubation for thoracic surgery. ASA physical status classification 2-4. Female patients aged 20-85 with a height of 160cm or less and a body mass index (BMI) of 25.0 kg/m2 or higher. Patients requiring VentiBroncTM Anchor 33Fr or Shiley® 32Fr intubation due to a left mainstem bronchus diameter of 11mm or less on chest CT. Exclusion Criteria: Intraluminal lesions in the left or right mainstem bronchi. History of airway surgery. Emergency surgery.

Locations (1)

Severance hospital

Seoul, South Korea

Outcomes

Primary Outcomes

Success rate of endobronchial intubation

Success or failure of endobronchial intubation will be determined immediately after double-lumen tube intubation, with flexible fiberoptic bronchoscope.

Time frame: Immediately after double-lumen tube intubation, with flexible fiberoptic bronchoscope

Data from ClinicalTrials.gov

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