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Role of Point of Care Ultrasound in Endotracheal Tube Placement

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04216199
Recruitment Status : Recruiting
First Posted : January 2, 2020
Last Update Posted : January 2, 2020
Sponsor:
Information provided by (Responsible Party):
Sherief Abd-Elsalam, Tanta University

Brief Summary:
Role of point of care ultrasound in endotracheal tube placement in children

Condition or disease Intervention/treatment Phase
Endotracheal Tube Wrongly Placed During Anesthetic Procedure Device: Point of care Ultrasound Not Applicable

Detailed Description:
Role of point of care ultrasound in confirmation of endotracheal tube placement in children

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 40 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Role of Point of Care Ultrasound in Confirmation of Endotracheal Tube Placement in Children
Actual Study Start Date : November 1, 2019
Estimated Primary Completion Date : December 1, 2030
Estimated Study Completion Date : December 20, 2030

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Ultrasound

Arm Intervention/treatment
Experimental: Point of care Ultrasound
Point of care Ultrasound for placement of endotracheal tube
Device: Point of care Ultrasound
Point of care Ultrasound
Other Name: POC Ultrasound

No Intervention: Traditional
Traditional method of insertion of endotracheal tube



Primary Outcome Measures :
  1. Number of patients with correct placement of endotracheal tube [ Time Frame: 6 months ]
    The number of patients with correct placement of endotracheal tube



Information from the National Library of Medicine

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Ages Eligible for Study:   up to 18 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Children below 18 years needing endotracheal intubation.

Exclusion Criteria:

  • Age more than 18 years.
  • Patients with significant neck or lung pathology.
  • Patients with elective intubation

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04216199


Contacts
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Contact: Sherief Abd-Elsalam, ass. prof. 00201147773440 sheriefabdelsalam@yahoo.com

Locations
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Egypt
Sherief Abd-Elsalam Recruiting
Tanta, Egypt
Contact: Sherief Abd-Elsalam, Ass. Prof.    00201009221243    sheriefabdelsalam@yahoo.com   
Sponsors and Collaborators
Sherief Abd-Elsalam
Investigators
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Principal Investigator: Fekry khater, Msc Emergency medicine department - Alazhar University
Principal Investigator: Mohamed S Sharaf, Prof. Anasthesia and Pain department - Alazhar University
Study Director: Mohamed H Elshafey, Prof Radiodiagnosis Department - Tanta University
Study Director: Mohamed G Elbahnasawy, Lecturer Emergency medicine department - Tanta University
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Responsible Party: Sherief Abd-Elsalam, Ass. Prof. Tropical Medicine, Tanta University
ClinicalTrials.gov Identifier: NCT04216199    
Other Study ID Numbers: elbahnasawy
First Posted: January 2, 2020    Key Record Dates
Last Update Posted: January 2, 2020
Last Verified: December 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No