NCT06061055View on ClinicalTrials.gov

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

NACompletedINTERVENTIONAL
Enrollment

154

Participants

Timeline

Start Date

October 26, 2023

Primary Completion Date

November 26, 2024

Study Completion Date

November 26, 2024

Conditions
Endotracheal Intubation
Interventions
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).

Trial Locations (1)

Unknown

Severance hospital, Seoul

All Listed Sponsors
lead

Yonsei University

OTHER

NCT06061055 - Comparison of VentiBroncTM Anchor With Conventional Double-lumen Endobronchial Tube in Patients With High Risk of Malposition | Biotech Hunter | Biotech Hunter