Skip to main content
Clinical Trials/NCT05399108
NCT05399108
Completed
Not Applicable

Ultrasound-guided Vena Jugularis Interna Catheterization Lateral Approach Short Axis in - Plane Technique

Masarykova Nemocnice v Usti nad Labem, Krajska Zdravotni a.s.1 site in 1 country200 target enrollmentJuly 25, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Central Vein Catheter
Sponsor
Masarykova Nemocnice v Usti nad Labem, Krajska Zdravotni a.s.
Enrollment
200
Locations
1
Primary Endpoint
Success rate of first attempt
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Central venous access is one of the most frequently used venous accesses in intensive care units. Insertion of the central venous catheter belongs to the basic skills of an intensivist. One of the veins that are available for catheterization is the internal jugular vein. It is recommended to perform jugular vein catheterization along with real-time ultrasound guidance.

Imaging of the jugular vein is usually performed in two ways: on the short axis or on the long axis. The puncture method is described based on the type of needle imaging technique, out-of-plane or in-plane method.

Traditionally, catheterization is performed by a medium approach during imaging the vein on a short axis using the out-of-plane technique. The main advantage of this procedure is proper imaging of the jugular vein and surrounding anatomical structures. However, the limited needle display is rather inconvenient, as only the needle tip can be displayed. This method of central venous catheterization has a first attempt success rate of 80%.

This study is going to concentrate on discussing the performing of jugular vein catheterization by a novel lateral approach in-plane technique during imaging of the vein on the short axis. This procedure for placement of a central venous catheter into the internal jugular vein has not yet been described nor investigated. The above-mentioned method combines the advantage of reliable jugular vein imaging together with proper imaging of the whole needle. At the same time, the fixation of the catheter in the supraclavicular region allows for a better nursing routine, hence increasing the patient's comfort.

Detailed Description

All potential candidates to enroll will undergo an examination by an anesthetist. If the candidate meets inclusion/ exclusion criteria, the candidate will sign an informed consent and be enrolled in the study. The calculated number of needed subjects is 180 (90 in each group). In the next step, all enrolled subjects will be randomized by computer block randomization into two groups. * In group A catheterization of vena jugularis interna will be done by lateral approach with visualization of the vein on its short axis with ultrasound and the in-plane technique will be used. * In group B catheterization of the vena jugularis interna will be done by conventional approach with visualization of the vein on its short axis with ultrasound and the out-of-plane technique will be used. Later then all enrolled subjects will undergo examination by an anesthetist or neurologist focused on neurological deficits in the upper limbs. The assessment will be done by Neurological Impairment Scale (NIS). In the next step catheterization of the vein will be done according to the latest international recommendations and the randomized group. The time of the start of catheterization and the time of the end of catheterization will be recorded. On daily basis, there will be done function control of the central vein catheter. The control is done by aspiration from all accesses. Unproblematic aspiration from all accesses will be interpreted as a functional catheter. On daily basis, there will be done ultrasound control of the catheter to evaluate the presence of thrombosis. On daily basis, there will be control of the insertion site of the catheter any complications such as signs of an infection or signs of catheter damage will be recorded. Before extraction of the catheter, there will be examined by an anesthetist or neurologist to evaluate neurological impairment in the upper limbs. The reason and the date of the extraction of the catheter will be recorded. All measured data will be recorded on the case report form and also will be recorded in the patient's hospital medical documentation. The recorded data will be processed by standard statistical tests such as T-tests and students test. The aim of this study is to prove the noninferiority of the novel lateral approach.

Registry
clinicaltrials.gov
Start Date
July 25, 2022
End Date
January 30, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Masarykova Nemocnice v Usti nad Labem, Krajska Zdravotni a.s.
Responsible Party
Principal Investigator
Principal Investigator

Michal Kalina

Principal Investigator

Masarykova Nemocnice v Usti nad Labem, Krajska Zdravotni a.s.

Eligibility Criteria

Inclusion Criteria

  • Patient older than 18 years with an indication of central venous catheter placement

Exclusion Criteria

  • Not signing the informed consent
  • BMI under 16,5
  • Contraindication of central venous catheter placement into internal jugular vein (thrombosis, site infection, bleeding diseases, anticoagulation or antiaggregation therapy)
  • hypersensitivity to sterile ultrasound gel
  • neurological impairment on upper limbs
  • neurodegenerative disorder

Outcomes

Primary Outcomes

Success rate of first attempt

Time Frame: Measured from the time the cannulation starts (local anesthetic infiltration) till insertion of the catheter, up to 120 minutes.

Primary outcome is to prove that first attempt success rate by the novel approach is comparable with the success rate of the first attempt success rate of the conventional approach.

Secondary Outcomes

  • Functional time of the catheter(Measured from inserting the catheter till the extraction of the catheter, up to 45 days.)
  • Rate of complications(Measured from the start of cannulation (local anesthetic infiltration) till extraction of the catheter, up to 45 days.)
  • Risk of neurological impairment assessed by Neurological Impairment Scale(Measured from insertion the catheter till the extraction of the catheter, up to 45 days.)

Study Sites (1)

Loading locations...

Similar Trials