The Ability of Anesthesiologists Identifying Internal Jugular Vein Bilaterally by Anatomic Landmarks

June 10, 2016 updated by: derya özkan, Diskapi Teaching and Research Hospital

The Ability of Anesthesiologists Identifying Internal Jugular Vein by Anatomic Landmark Technique

The study is designed to determine anaesthetists ability to locate the right internal jugular vein(IJV) and left IJV using a landmark technique. Initially, a questionnaire was completed detecting previous user experience. An ultrasound probe, using the midpoint as an 'imaginary needle', was placed on the neck of a healthy volunteer and the image recorded. Both anaesthetist and volunteer were blinded to the screen until the image was stored. Anaesthetists were grouped into senior or junior by the total number of IJV canulation experience. The success rate is going to be measured as pass or fail.

Study Overview

Detailed Description

Anesthesiologists are usually qualified in internal jugular vein canulation by using anatomic landmark technique. The anatomy of right IJV and left IJV may differ each other. The hypothesis is that the anatomical difference between right and left IJV may give rise to false puncture of especially left IJV by using anatomical landmark technique.Although USG is available, most of the experienced anesthesiologist does not prefer to use USG for IJV canulation due to different reasons.In addition to this anesthesiologists are generally preferring right IJV canulation, thus they are inexperienced in left IJV canulation. So especially during left IJV canulation,not by anatomical landmark technique but by USG will be recommended for anesthesiologists.

Study Type

Observational

Enrollment (Actual)

50

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

    • Altindag
      • Ankara, Altindag, Turkey, 06130
        • Ministry of health diskapi yildirim beyazit training and research hospital

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

22 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

the residents of anesthesiology clinics

Description

Inclusion Criteria:

  • The voluntary anesthesiologists who are studying in diskapi training and research hospital

Exclusion Criteria:

  • The anesthesiologists who are not willing to participate, the anesthesiologists whom refused to fulfill the questionnaire form.

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

Cohorts and Interventions

Group / Cohort
anesthesiologists, experience
There is one arm. All participating anesthesiologists wıll fulfill the questionary survey and show the imaginary puncture site by USG bilaterally.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
determine the difference between anesthesiologists ability to show left and right internal jugular vein by usg probe (pass/fail)
Time Frame: participants will be followed for the duration of operating room stay, an expected average of 15 minutes
The participants are going to be graded pass/fail according to whether the midline trajectory of the usg probe intersected any part of the lumen of the internal jugular vein. The participating anesthesiologists will show imaginary puncture site for IJV cannulation bilaterally by ultrasonography. The blind investigator will save the ultrasonographic images as jpeg files and another investigator will consider the images.
participants will be followed for the duration of operating room stay, an expected average of 15 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
determine the difference between senior and junior anesthesiologists ability to show left and right internal jugular vein by usg probe (pass/fail).
Time Frame: participants will be followed for the duration of operating room stay, an expected average of 15 minutes
The participants are going to fulfill a survey asking their experience about IJV canulation. After the survey the anesthesiologists are going to classified as senior/junior. The participants are going to be graded pass/fail according to whether the midline trajectory of the usg probe intersected any part of the lumen of the internal juguler vein.
participants will be followed for the duration of operating room stay, an expected average of 15 minutes

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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

June 1, 2012

Primary Completion (Actual)

July 1, 2012

Study Completion (Actual)

July 1, 2012

Study Registration Dates

First Submitted

May 18, 2012

First Submitted That Met QC Criteria

May 29, 2012

First Posted (Estimate)

May 30, 2012

Study Record Updates

Last Update Posted (Estimate)

June 13, 2016

Last Update Submitted That Met QC Criteria

June 10, 2016

Last Verified

May 1, 2012

More Information

Terms related to this study

Other Study ID Numbers

  • DiskapiTRH1
  • DiskapiTRH232012 (Registry Identifier: USGIJV232012)
  • USGIJV062012 (Registry Identifier: DiskapiTRH062012)

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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