The Depth of Endotracheal Tube Insertion

January 14, 2020 updated by: Gao Mei

An Observational Study of The Depth of Endotracheal Tube Insertion

Virtual experiment : comparing the new method with conventional method of determining the depth of endotracheal intubation.

Study Overview

Status

Completed

Detailed Description

Effective airway management is the primary concern of the anesthesiologist. The conventional method of determining the insertion length of the endotracheal tube, 21 cm for women and 23 cm for men, shows a high incidence of endobronchial intubations in the analyzed population.The aim of this study is form a new and safe practice habit by passing the endotracheal tube with the balloon just 2 cm below the vocal cords during intubation.

Study Type

Observational

Enrollment (Actual)

200

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Jiangsu
      • Nanjing, Jiangsu, China, 210029
        • The First Affiliated Hospital with Nanjing Medical University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

adult patients who are scheduled for elective surgery under general anesthesia

Description

Inclusion Criteria:

  • Patients who are scheduled for elective surgery under general anesthesia

Exclusion Criteria:

  • Patients with anatomical defects of the face, neck, or upper airway
  • Patients at risk for pulmonary aspiration of gastric content

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
the depth of primary insertion of tracheal tube
Time Frame: in a minute after intubation
in a minute after intubation

Secondary Outcome Measures

Outcome Measure
Time Frame
the distance from the corner of mouth to the carina
Time Frame: in a minute after intubation
in a minute after intubation
the distance from the vocal cords to the carina
Time Frame: in a minute after intubation
in a minute after intubation
the distance from the corner of mouth to the vocal cords
Time Frame: in a minute after intubation
in a minute after intubation

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 20, 2019

Primary Completion (Actual)

December 26, 2019

Study Completion (Actual)

December 26, 2019

Study Registration Dates

First Submitted

March 15, 2019

First Submitted That Met QC Criteria

March 15, 2019

First Posted (Actual)

March 18, 2019

Study Record Updates

Last Update Posted (Actual)

January 18, 2020

Last Update Submitted That Met QC Criteria

January 14, 2020

Last Verified

January 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • 2019-SR-041

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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