- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01607281
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
Status
Completed
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
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Altindag
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Ankara, Altindag, Turkey, 06130
- Ministry of health diskapi yildirim beyazit training and research hospital
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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 |
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anesthesiologists, experience
There is one arm.
All participating anesthesiologists wıll fulfill the questionary survey and show the imaginary puncture site by USG bilaterally.
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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
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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.
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participants will be followed for the duration of operating room stay, an expected average of 15 minutes
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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
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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.
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participants will be followed for the duration of operating room stay, an expected average of 15 minutes
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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.
General Publications
- Sulek CA, Blas ML, Lobato EB. A randomized study of left versus right internal jugular vein cannulation in adults. J Clin Anesth. 2000 Mar;12(2):142-5. doi: 10.1016/s0952-8180(00)00129-x.
- Harber CR, Harvey DJ, Wiles MD, Bogod DG. The ability of anaesthetists to identify the position of the right internal jugular vein correctly using anatomical landmarks. Anaesthesia. 2010 Sep;65(9):885-8. doi: 10.1111/j.1365-2044.2010.06426.x.
- Muralidhar K. Left internal versus right internal jugular vein access to central venous circulation using the Seldinger technique. J Cardiothorac Vasc Anesth. 1995 Feb;9(1):115-6. doi: 10.1016/s1053-0770(05)80084-9. No abstract available.
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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