Comparison of Double-lumen Tube Intubation Between Fiberoptic Bronchoscopy and Video Laryngoscope
Effect of Combined Use of Flexible Bronchoscope on First-attempt Sucess in Tracheal Double Lumen Tube Intubation Using Videolaryngosocpe: A Randomized Controlled Trial
1 other identifier
interventional
130
1 country
1
Brief Summary
The goal of this clinical trial is to compare the first-attempt success rate in double-lumen tube intubation. The main question it aims to answer: Is there any difference in the first-attempt success rate of intubation between using flexible bronchoscopy and a video laryngoscope? Researchers will compare the group using a flexible bronchoscope and video laryngoscope with the group using a video laryngoscope only to see if there is a difference in first-attempt success rate. Participants will be intubated in one of two interventions.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Nov 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 16, 2025
CompletedStudy Start
First participant enrolled
November 20, 2025
CompletedFirst Posted
Study publicly available on registry
November 21, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
November 25, 2026
December 23, 2025
December 1, 2025
12 months
November 16, 2025
December 20, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
first attempt success rate
The proportion of successful intubation at the first attempt
from enrollment to the end of tracheal intubation
Study Arms (2)
VL
NO INTERVENTIONDLT intubation using video laryngoscope only
VL+FOB
ACTIVE COMPARATORDLT intubation using video laryngoscope and fiberoptic bronchoscope
Interventions
Eligibility Criteria
You may qualify if:
- Scheduled operation
- Patients required to double lumen tube insertion for thoracic surgery
- ASA PS 1, 2, 3
You may not qualify if:
- BMI \<18.5 or 35.0
- history of airway surgery
- suspicious of high aspiration risk
- Pathology in oropharynx or larynx such as tumor, poly, or inflammation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Kyung Hee University Hospital at Gangdong
Seoul, 06090, South Korea
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MD, PhD
Study Record Dates
First Submitted
November 16, 2025
First Posted
November 21, 2025
Study Start
November 20, 2025
Primary Completion (Estimated)
October 31, 2026
Study Completion (Estimated)
November 25, 2026
Last Updated
December 23, 2025
Record last verified: 2025-12