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Comparison of Double Lumen Tube Location Verification Techniques in Single Lung Ventilation

K

Kayseri City Hospital

Status

Completed

Conditions

Lung Diseases
Lung Cancer

Treatments

Device: double lumen tube with video

Study type

Observational

Funder types

Other

Identifiers

NCT07107893
2024-KEAK-01

Details and patient eligibility

About

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).

Full description

The single-center, prospective and observational study included 93 patients aged 18-84 years, American Society of Anesthesiology (ASA) I-III, who were to undergo one-lung ventilation in the lateral decubitus position by thoracic surgery under elective conditions. Patients were randomized into Group I: Group with confirmed tube location by auscultation, Group II: Group with confirmed tube location by FOB and Group III: The group in which double lumen tube with video was used. Demographic data of the patients, intubation times, tube site confirmation times, number of type dislocation, dislocation correction time, number and duration of FOB use, quality of lung deflation, presence of postoperative sore throat and hoarseness were recorded. The three groups were compared in terms of cost.

Enrollment

93 patients

Sex

All

Ages

18 to 84 years old

Volunteers

No Healthy Volunteers

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

Trial design

93 participants in 3 patient groups

grup I
Description:
Group with confirmed tube location by auscultation
Grup II
Description:
Group with confirmed tube location by fiberoptic bronchoscope
Grup III
Description:
The group in which double lumen tube with video was used
Treatment:
Device: double lumen tube with video

Trial documents
3

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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