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Endotracheal IntubationNCT07669259

Bedside Ultrasound for Confirmation of Endotracheal Tube Placement in the Emergency Department

An observational study of Endotracheal Intubation and Endotracheal Tube Placement, run by Antalya Health Sciences University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 years and older
How many people
70 participants
Where
1 siteTurkey (Türkiye)
Study dates
10 Jan 2025to 10 Jun 2026
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: The study population consisted of adult patients aged 18 years or older who presented to the Emergency Department of Antalya Training and Research Hospital and underwent endotracheal intubation as part of routine emergency care. Patients were included after ethics committee approval if bedside ultrasound and capnometric end-tidal carbon dioxide assessment were performed for confirmation of endotracheal tube placement.

Who may be able to join

  • 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

Who cannot join

  • Patients younger than 18 years of age
  • Patients with missing or incomplete study data
  • Patients with ultrasound images of insufficient quality for evaluation

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • University of Health Sciences, Antalya Training and Research Hospital

    Antalya, konyaaltı, 07100

Other trials in Turkey (Türkiye)

About this study

Official title: 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.

Read the 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.

Keywords
Bedside ultrasound, Point-of-care ultrasound, Endotracheal tube placement, Capnography, Endotracheal tube confirmation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07669259
Study groupRoleWhat they receive
Patients Undergoing Endotracheal Intubation in the Emergency DepartmentAdult 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.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Diagnostic Accuracy of Bedside Ultrasound for Confirmation of Endotracheal Tube Placement

    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.

    Measured: During or immediately after endotracheal intubation, within a maximum of 20 seconds

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Jun 2026
  2. Study start10 Jan 2025
  3. Primary completion10 Jun 2026
  4. Study completion10 Jun 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
70 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07669259
Sponsor's protocol ID
2025-019
Status last verified
Jun 2026
First submitted
20 Jun 2026
Last updated
25 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data will not be shared publicly because the study includes clinical data from emergency department patients and there may be confidentiality and institutional restrictions. De-identified aggregate results will be reported in scientific publications.

Publications

  • Long B, Koyfman A, Gottlieb M. Diagnostic Accuracy of Ultrasound for Confirmation of Endotracheal Tube Placement. Acad Emerg Med. 2019 Sep;26(9):1096-1098. doi: 10.1111/acem.13773. Epub 2019 May 23. No abstract available.

    PubMed 31046166

Questions about this trial

What is this clinical trial studying?

An observational study of Endotracheal Intubation and Endotracheal Tube Placement, run by Antalya Health Sciences University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 25 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

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). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07669259, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Jun 2026.

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