- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04740385
Role of Lung Ultrasound in Confirmation of Correct Double Lumen Endotracheal Tube Placement in Thoracic Surgeries
July 16, 2022 updated by: Walaa Youssef Elsabeeny, National Cancer Institute, Egypt
Role of Transthoracic Lung Ultrasound in Confirmation of Correct Double Lumen Endotracheal Tube
to assess the efficacy of lung ultrasound versus conventional auscultation method and fiberoptic bronchoscopy in confirmation of double lumen tube position
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed 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
Study Type
Observational
Enrollment (Actual)
117
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Cairo, Egypt, 11796
- Department of anesthesia and pain medicine. National Cancer Institute
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
lung cancer patients undergoing thoracic surgeries requiring double lumen intubation
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Lung cancer patients
Correct position of double lumen endotracheal tube will be assessed using lung sonography, routine chest auscultation and fiberoptic brochoscopy
|
auscultation of air entry through chest wal
Checking correct double lumen position through direct vision using fiberoptic bronchoscopy
real time visualization of air entry to the lungs using trans-thoracic lung ultrasound
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
sensitivity and specificity of lung ultrasound in confirmation of correct double lumen position
Time Frame: 5 minutes
|
real time visulaization of air entry to the lung
|
5 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
procedural time
Time Frame: 5 minutes
|
time taken to confirm tube position
|
5 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 3, 2021
Primary Completion (Actual)
June 25, 2022
Study Completion (Actual)
June 30, 2022
Study Registration Dates
First Submitted
February 1, 2021
First Submitted That Met QC Criteria
February 1, 2021
First Posted (Actual)
February 5, 2021
Study Record Updates
Last Update Posted (Actual)
July 19, 2022
Last Update Submitted That Met QC Criteria
July 16, 2022
Last Verified
July 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- 202101-2P-02002
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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