NCT07107893Completed
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 · Last updated 6 Aug 2025
Brief summary (registry, in English)
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).
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 93 (actual)
- First submitted
- 17 Jul 2025
- Start date
- 16 Jan 2025
- Primary completion date
- 15 Apr 2025
- Lead sponsor
- Kayseri City Hospital
- Diseases
- Lung cancer
- NCT number
- NCT07107893
What you commit to
- Study type: Observational
- Participants enrolled: 93
- From 16 Jan 2025 to the primary completion date, 15 Apr 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients undergoing emergency surgery
Other illness
- Patients with uncontrolled metabolic disease
Other
- 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)
- Mentally retarded patients
- Patients under 18 or over 84
- Patients with tracheal or airway abnormalities
- Pregnant or breastfeeding women
Who the study is looking for
- Patients who will undergo TAV and be placed in the lateral position.
- Patients with ASA scores of I-III.
- Patients aged 18-84.
Age in the registry: 18 years to 84 years · Sex: All
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Kayseri Şehir Hastanesi Coordinator of this site? Confirm its status | Kayseri | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.