Comparison of Double Lumen Tube Location Verification Techniques in Single Lung Ventilation
NCT ID: NCT07107893
Last Updated: 2025-08-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
93 participants
OBSERVATIONAL
2025-01-16
2025-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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grup I
Group with confirmed tube location by auscultation
No interventions assigned to this group
Grup II
Group with confirmed tube location by fiberoptic bronchoscope
No interventions assigned to this group
Grup III
The group in which double lumen tube with video was used
double lumen tube with video
Methods used to confirm tube placement in one-lung ventilation: auscultation, fiberoptic bronchoscopy, and video to evaluate double-lumen tube use
Interventions
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double lumen tube with video
Methods used to confirm tube placement in one-lung ventilation: auscultation, fiberoptic bronchoscopy, and video to evaluate double-lumen tube use
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Patients with ASA scores of I-III.
* Patients aged 18-84.
Exclusion Criteria
* 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
18 Years
84 Years
ALL
No
Sponsors
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Kayseri City Hospital
OTHER_GOV
Responsible Party
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Arzu Fırat Durbilmez
assistant doctor of anesthesiology and reanimation
Locations
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Kayseri Şehir Hastanesi
Kayseri, Kocasinan, Turkey (Türkiye)
Countries
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Provided Documents
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Document Type: Study Protocol: RESEARCH PROTOCOL
Document Type: Statistical Analysis Plan: STATISTICAL ANALYSIS
Document Type: Informed Consent Form: INFORMED VOLUNTARY CONSENT FORM
Other Identifiers
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2024-KEAK-01
Identifier Type: -
Identifier Source: org_study_id
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