- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07669259
Bedside Ultrasound for Confirmation of Endotracheal Tube Placement in the Emergency Department
The Role of Bedside Ultrasound in Confirming Endotracheal Tube Placement in Patients Undergoing Endotracheal Intubation in the Emergency Department
This prospective observational study evaluated the role of bedside ultrasound in confirming endotracheal tube placement in adult patients who underwent endotracheal intubation in the emergency department. Correct placement of the endotracheal tube is critical because unrecognized incorrect placement may cause hypoxemia, hypoxic brain injury, or death.
In this study, bedside ultrasound was performed during or immediately after endotracheal intubation without interfering with the intubation procedure. Ultrasound findings were compared with capnographic end-tidal carbon dioxide measurement, which was used as the reference method for confirming tube placement. The main aim was to assess whether bedside ultrasound is a useful and reliable method for confirming endotracheal tube position in emergency department patients.
Study Overview
Status
Detailed Description
This single-center, prospective observational diagnostic accuracy study was conducted in the Emergency Department of Antalya Training and Research Hospital. Adult patients who underwent endotracheal intubation in the emergency department after ethics committee approval were included.
Endotracheal intubation was performed as part of routine emergency care by the most senior emergency medicine resident or an experienced emergency physician. Bedside ultrasound assessment was performed during or immediately after intubation by trained emergency physicians without interrupting or delaying the intubation procedure. The ultrasound examination was performed from the suprasternal notch region to assess the position of the endotracheal tube.
The physicians who performed bedside ultrasound had at least two years of emergency medicine experience and had completed accredited ultrasound training. Before study data collection, they received additional theoretical and practical training focused on ultrasound confirmation of endotracheal tube placement.
Ultrasound findings were compared with capnometric end-tidal carbon dioxide measurement, which was used as the reference method for confirmation of endotracheal tube placement. Ultrasound images were stored in the hospital computer system and reviewed by two qualified, independent radiology specialists. Images or measurements with insufficient quality were excluded from analysis. Agreement between ultrasound assessments was evaluated statistically.
The study aimed to determine whether bedside ultrasound can be used as a rapid, reliable, and practical method for confirming endotracheal tube placement in emergency department patients.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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konyaaltı
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Antalya, konyaaltı, Turkey (Türkiye), 07100
- University of Health Sciences, Antalya Training and Research Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients aged 18 years or older
- Patients who underwent endotracheal intubation in the emergency department as part of routine emergency care
- Patients in whom bedside ultrasound and capnometric end-tidal carbon dioxide assessment were performed for confirmation of endotracheal tube placement
Exclusion Criteria:
- Patients younger than 18 years of age
- Patients with missing or incomplete study data
- Patients with ultrasound images of insufficient quality for evaluation
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Patients Undergoing Endotracheal Intubation in the Emergency Department
Adult patients who underwent endotracheal intubation in the emergency department were included in this cohort.
Endotracheal intubation was performed as part of routine emergency care.
Bedside ultrasound was performed during or immediately after intubation by trained emergency physicians without interrupting the procedure.
Ultrasound findings were compared with capnometric end-tidal carbon dioxide measurement, which was used as the reference method for confirming endotracheal tube placement.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Diagnostic Accuracy of Bedside Ultrasound for Confirmation of Endotracheal Tube Placement
Time Frame: During or immediately after endotracheal intubation, within a maximum of 20 seconds
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The diagnostic accuracy of bedside ultrasound for confirming endotracheal tube placement will be evaluated by comparing ultrasound findings with capnometric end-tidal carbon dioxide measurement, which will be used as the reference method.
Diagnostic performance will be assessed using sensitivity, specificity, positive predictive value, negative predictive value, overall accuracy, and agreement with the reference method.
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During or immediately after endotracheal intubation, within a maximum of 20 seconds
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Collaborators and Investigators
Investigators
- Principal Investigator: MURAT DUYAN, ASSOCIATE PROFESSOR, University of Health Sciences, Antalya Training and Research Hospital
- Study Director: HALIT EKICI, MEDICAL DOCTOR, University of Health Sciences, Antalya Training and Research Hospital
- Study Director: CEMIL KAVALCI, PROFESSOR, University of Health Sciences, Antalya Training and Research Hospital
- Study Director: ENGIN DENIZ ARSLAN, ASSOCIATE PROFESSOR, University of Health Sciences, Antalya Training and Research Hospital
- Study Director: FEVZI YILMAZ, University of Health Sciences, Antalya Training and Research Hospital
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2025-019
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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