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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03081221
Other study ID # 60-68
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 2016
Est. completion date July 2018

Study information

Verified date February 2019
Source Cukurova University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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


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.


Recruitment information / eligibility

Status Completed
Enrollment 64
Est. completion date July 2018
Est. primary completion date June 2017
Accepts healthy volunteers No
Gender All
Age group N/A to 18 Years
Eligibility Inclusion Criteria:

- applied intubation patients

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
USG


Locations

Country Name City State
Turkey Cukurova University Adana

Sponsors (1)

Lead Sponsor Collaborator
Cukurova University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Detection of Tube Tube shall be detected with Ultrasonography (USG) 1 year
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