Success of Internal Jugular Vein Catheterization

February 4, 2023 updated by: Bengü Gülhan Köksal, Zonguldak Bulent Ecevit University

Factors Affecting Success of First Attempt in Ultrasonography-Guided Internal Jugular Vein Catheterization

Internal jugular vein cannulation can be performed with the blind technique under ultrasound (USG) guidance or using classical marker points. It has been shown that USG-guided interventions reduce the complication rate compared to the method performed with the blind technique (4%/13.5%). In addition, the initial entry success rate in the USG supported group is 65%. , this rate remained at 45% with the blind technique.

Although Pleth variability index monitoring is a noninvasive method, it is a technique that consistently predicts fluid sensitivity in patients under mechanical ventilation.

The aim of study is before applying USG guided catheterization; We think that by revealing the factors of the patient that are effective on the number of interventions, necessary measures can be taken for the success of catheterization as a result.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

1

Phase

  • Not Applicable

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

  • Turkey
    • Esenköy
      • Kozlu, Esenköy, Turkey, 67600
        • Zonguldak Bülent Ecevit University Faculty of Medicine
    • Kozlu
      • Zonguldak, Kozlu, Turkey, 67600
        • Zongulak Bülent Ecevit 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 75 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • aged 18-75
  • underwent coronary artery bypass surgery

Exclusion Criteria:

  • <18 years old
  • Hemodynamic instability
  • Use of inotropic agents

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

  • Primary Purpose: SUPPORTIVE_CARE
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
ACTIVE_COMPARATOR: single attempt catheterization
successful catheterization with a single attempt number
Procedure: Internal Jugular Vein Catheterization
Inserting a cannula into the internal jugular vein
ACTIVE_COMPARATOR: multiple attempts catheterization
successful catheterization after multiple attempts
Procedure: Internal Jugular Vein Catheterization
Inserting a cannula into the internal jugular vein

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
factors of internal vein jugular catheterization success
Time Frame: Baseline (Before catheterization)
neck circumference,
Baseline (Before catheterization)
factors of internal vein jugular catheterization success
Time Frame: Baseline (Before catheterization)
internal juguler vein depth
Baseline (Before catheterization)
factors of internal vein jugular catheterization success
Time Frame: Baseline (Before catheterization)
internal vein diameter
Baseline (Before catheterization)
factors of internal vein jugular catheterization success
Time Frame: Baseline (Before catheterization)
pleth variability index
Baseline (Before catheterization)

Collaborators and Investigators

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

Sponsor

Zonguldak Bulent Ecevit University

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)

January 1, 2019

Primary Completion (ACTUAL)

December 31, 2020

Study Completion (ACTUAL)

January 1, 2022

Study Registration Dates

First Submitted

January 31, 2023

First Submitted That Met QC Criteria

February 4, 2023

First Posted (ACTUAL)

February 8, 2023

Study Record Updates

Last Update Posted (ACTUAL)

February 8, 2023

Last Update Submitted That Met QC Criteria

February 4, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 2018/12-6

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

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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