Verification of Endotracheal Tube Placement With Ultrasonography (USG)

• Sponsor: Cukurova University (Other)
• Overall Status: Completed
• CT.gov ID: NCT03081221
• Collaborator: (none)
• Enrollment: 64
• Location: 1
• Actual Duration (Months): 25
• Patients Per Site Per Month: 2.6

Study Details

Study Description

Brief Summary

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

Condition or Disease	Intervention/Treatment	Phase
Intubation	Diagnostic Test: USG

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.

Study Design

• Study Type: Observational [Patient Registry]
• Actual Enrollment: 64 participants
• Observational Model: Cohort
• Time Perspective: Cross-Sectional
• Official Title: Verification of Endotracheal Tube Placement With Ultrasonography (USG) in Patients
• Actual Study Start Date: Jun 1, 2016
• Actual Primary Completion Date: Jun 1, 2017
• Actual Study Completion Date: Jul 1, 2018

Outcome Measures

Primary Outcome Measures

1. Detection of Tube [1 year]

   Tube shall be detected with Ultrasonography (USG)

Eligibility Criteria

Criteria

• Ages Eligible for Study: N/A to 18 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• applied intubation patients

Exclusion Criteria:

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Cukurova University	Adana		Turkey

Sponsors and Collaborators

• Cukurova University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Ozlem Tolu Kendir, Fellow, Cukurova University
• ClinicalTrials.gov Identifier: NCT03081221
• Other Study ID Numbers: 60-68
• First Posted: Mar 16, 2017
• Last Update Posted: Feb 4, 2019
• Last Verified: Feb 1, 2019

• Individual Participant Data (IPD) Sharing Statement: Undecided
• Plan to Share IPD: Undecided
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

Study Results

No Results Posted as of Feb 4, 2019