Clinical trial · Observational
Comparison of Double Lumen Tube Location Verification Techniques in Single Lung Ventilation
Comparison of Double Lumen Tube Location Verification Techniques in Single Lung Ventilation: Auscultation, Fiberoptic Bronchoscopy, and Video Double Lumen Tube
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The aim of this study was to compare auscultation, fiberoptic bronchoscopy (FOB) and video double lumen tube (VDLT) double lumen tube (DLT) location confirmation techniques in terms of intraoperative tube location confirmation time, number of tube dislocations, correction time of dislocations, FOB usage rates, lung deflation quality, postoperative sore throat, presence of hoarseness and cost in thoracic surgery patients undergoing one lung ventilation (OLV).
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Lung Cancer | Malignant Lung Neoplasm | CURATED_EXACT | 0.92 |
| Lung Diseases | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| double lumen tube with video | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- label
- grup I
- description
- Group with confirmed tube location by auscultation
- label
- Grup II
- description
- Group with confirmed tube location by fiberoptic bronchoscope
- label
- Grup III
- description
- The group in which double lumen tube with video was used
- interventionNames
- Device: double lumen tube with video
Primary outcomes (1)
- measure
- verification of tube location
- timeFrame
- during surgery
- description
- The primary endpoint is the identification of a method that allows the quickest confirmation of double-lumen tube location after intubation and possible intraoperative location changes.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 84 Years
Show eligibility criteria text
Inclusion Criteria: * Patients who will undergo TAV and be placed in the lateral position. * Patients with ASA scores of I-III. * Patients aged 18-84. Exclusion Criteria: * Patients undergoing emergency surgery * Patients with American Society of Anesthesiology (ASA) IV and above * Patients with anticipated difficult intubation * Patients requiring intubation with a right thoracic duct (CLT) * Patients with more than three intubation attempts * Patients who refuse to participate in the study * Patients who will undergo TAV but will not be placed in the lateral position (sympathectomy) * Patients with uncontrolled metabolic disease * Mentally retarded patients * Patients under 18 or over 84 * Patients with tracheal or airway abnormalities * Pregnant or breastfeeding women
References
Publications (0)
Data not yet available