Status:
COMPLETED
Comparison of VentiBroncTM Anchor With Conventional Double-lumen Endobronchial Tube in Patients With High Risk of Malposition
Lead Sponsor:
Yonsei University
Conditions:
Endotracheal Intubation
Eligibility:
All Genders
20-85 years
Phase:
NA
Brief 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...
Eligibility Criteria
Inclusion
- 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
- Intraluminal lesions in the left or right mainstem bronchi. History of airway surgery. Emergency surgery.
Key Trial Info
Start Date :
October 26 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 26 2024
Estimated Enrollment :
154 Patients enrolled
Trial Details
Trial ID
NCT06061055
Start Date
October 26 2023
End Date
November 26 2024
Last Update
December 12 2024
Active Locations (1)
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1
Severance hospital
Seoul, South Korea