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CompletedNCT03081221Updated Feb 4, 2019

Verification of Endotracheal Tube Placement With Ultrasonography (USG)

An observational study in Intubation, sponsored by Cukurova University. Completed at 1 site in Turkey. Open to participants aged Up to 18 Years. Per ClinicalTrials.gov, last updated 2019-02-04.

Sponsored by Cukurova University · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
64
Ages
Up to 18 Years
Sex
All
01

Study summary

The purpose of this study is to verification of Endotracheal Tube Placement with Ultrasonography (USG).

Read the detailed description

The purpose of this study is to verification of Endotracheal Tube Placement with Ultrasonography (USG). In this study, using of USG during verification will be compared with traditional method.

In traditional methods, after intubation, verification of endotracheal tube placement is done via to monitoring of thorax movement, checking of tube fogging, auscultation of lung and stomach, capnography and radiography.

In USG method, after intubation, verification of endotracheal tube placement is done via to using linear transducer. The probe will be placed transversely and longitudinally on the neck and in front of cricoid cartilage.

So, collected all data from two method will be compared.

02

Conditions studied

  • Intubation
03

In context

Lead sponsor

Cukurova University is the lead sponsor of 247 studies on the registry; 50 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

0-18 age children

Inclusion criteria

  • applied intubation patients

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
64 participants (actual)
Target follow-up
1 Day
Patient registry
Yes

Interventions

  • Diagnostic testUSG
06

What researchers measure

Primary outcomes

  1. Detection of Tube

    Tube shall be detected with Ultrasonography (USG)

    Time frame: 1 year

07

Study locations

1 site
  • Cukurova University
    Adana, Turkey
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 4, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03081221
Lead sponsor
Cukurova University
Responsible party
Ozlem Tolu Kendir (Fellow, Cukurova University) — Principal investigator
First posted
Mar 16, 2017
Start date
Jun 2016
Primary completion
Jun 2017
Completion
Jul 2018
Last update
Feb 4, 2019

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2019. You cannot join it, but the record below documents what was studied.

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