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Impact of Patient Position on the Success in Placing Triple-cuffed Double Lumen Endotracheal Tube

NCT05462275 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 167

Last updated 2022-07-18

No results posted yet for this study

Summary

Triple-cuffed double lumen endotracheal tube (TC-DLT, ANKOR tube. Insung corp., Korea) which was developed to isolate lung without endotracheal bronchoscope guidance has additional carinal cuff placed between bronchial tube cuff and tracheal tube cuff. This device has been successfully used to isolate lung more simply in specific settings when there is too much excretion to visualize endotracheal structure or for a health provider who is not good at use of traditional double-lumen tube. Although TC-DLT is designed to enable lung separation effectively in situations that confirmation of tube position using bronchoscopy is difficult or not available, but no studies have been conducted on whether effective lung isolation using TC-DLT is possible after change in the relative position of the bronchial tree by postural change. This plan was prepared for research on this.

Conditions

  • Lung Diseases

Interventions

DEVICE

Intubation using 3-cuffed double lumen endotracheal tube

After patient's position, 3-cuffed double lumen endotracheal tube is intubated without fiberoptic bronchoscopy guidance

Sponsors & Collaborators

  • Hansu Bae

    lead OTHER

Principal Investigators

  • Dongkyu Lee · Department of anesthesiology, Dongguk University Il-san hospital

Study Design

Allocation
NA
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
19 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-04-29
Primary Completion
2023-04-29
Completion
2023-04-29

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05462275 on ClinicalTrials.gov