Actively Recruiting

Age: 18Years - 65Years
All Genders
NCT07465510

Ultrasound vs. Auscultation and Fiberoptic Bronchoscopy for Double-Lumen Tube Placement

Led by Izmir City Hospital · Updated on 2026-03-12

100

Participants Needed

1

Research Sites

20 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

One-lung ventilation is frequently required in thoracic surgery and is most commonly achieved using double-lumen endobronchial tubes (DLTs). Correct positioning of the DLT is crucial for effective lung isolation and patient safety. Fiberoptic bronchoscopy (FOB) is considered the gold standard for confirming DLT placement; however, it may not always be immediately available and requires specific expertise. Lung ultrasonography is a rapid, noninvasive, and bedside imaging method increasingly used in anesthesiology and critical care. This prospective observational study aims to evaluate the diagnostic performance of lung ultrasound in confirming the correct position of double-lumen endobronchial tubes in patients undergoing thoracic surgery. The results obtained from lung ultrasound will be compared with auscultation findings and fiberoptic bronchoscopy results. Fiberoptic bronchoscopy will be considered the reference standard. The sensitivity, specificity, positive predictive value, and negative predictive value of lung ultrasound and auscultation will be calculated.

CONDITIONS

Official Title

Ultrasound vs. Auscultation and Fiberoptic Bronchoscopy for Double-Lumen Tube Placement

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 65 years
  • Scheduled for elective thoracic surgery
  • Planned one-lung ventilation
  • Use of double-lumen endobronchial tube
  • ASA physical status I-III
  • Written informed consent obtained
Not Eligible

You will not qualify if you...

  • Known airway anomalies
  • Previous lung resection surgery
  • Tracheostomy
  • Coagulopathy
  • Pleural effusion or pleural pathology interfering with lung ultrasound evaluation
  • Chest wall deformity
  • Emergency surgery
  • Patients who decline participation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Izmir City Hospital

Izmir, İzmir, Turkey (Türkiye), 35150

Actively Recruiting

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Research Team

C

Cansu KATKAY, M.D.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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