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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04740385
Other study ID # 202101-2P-02002
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 3, 2021
Est. completion date June 30, 2022

Study information

Verified date July 2022
Source National Cancer Institute, Egypt
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

to assess the efficacy of lung ultrasound versus conventional auscultation method and fiberoptic bronchoscopy in confirmation of double lumen tube position


Description:

Confirmation of double lumen tube position by auscultation followed fiberoptic bronchoscopy then lung ultrasound. After double lumen intubation all patient tube position will be confirmed using auscultation then fiberoptic bronchoscopy then lung ultrasound


Recruitment information / eligibility

Status Completed
Enrollment 117
Est. completion date June 30, 2022
Est. primary completion date June 25, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - patients scheduled for surgeries under general anesthesia requiring double lumen endotracheal intubation - ASA I-II Exclusion Criteria: - patient refusal - patients not meeting the inclusion criteria

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Lung auscultation
auscultation of air entry through chest wal
Device:
Fiberoptic bronchoscopy
Checking correct double lumen position through direct vision using fiberoptic bronchoscopy
Lung Ultrasound
real time visualization of air entry to the lungs using trans-thoracic lung ultrasound

Locations

Country Name City State
Egypt Department of anesthesia and pain medicine. National Cancer Institute Cairo

Sponsors (1)

Lead Sponsor Collaborator
National Cancer Institute, Egypt

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary sensitivity and specificity of lung ultrasound in confirmation of correct double lumen position real time visulaization of air entry to the lung 5 minutes
Secondary procedural time time taken to confirm tube position 5 minutes
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