CClinicalTrials.gg
Active, not recruitingNCT06591234AIJV-IUpdated Sep 19, 2024

Reliability of Internal Jugular Ultrasound : an Observational Transversal Study Conducted Using Images Registered From Patients (AIJV-I)

An observational study in Hypervolemia and Hypovolemia, sponsored by Maggiore Bellaria Hospital, Bologna. Active, not recruiting at 1 site in Italy. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-09-19.

Sponsored by Maggiore Bellaria Hospital, Bologna · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2024, 1 year 9 months ago, but the record still lists the study as active, not recruiting.
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
10
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this observational study is to test the inter-rater reliability among a group of ultrasound measurements of internal jugular vein using a group of images, registered in several acoustic views of neck of patients admitted in Medicine Department.

The main questions it aims to answer is: are there differences in recording echographic measurements of the internal jugular vein between different sonographers ?

Read the detailed description

Dear Mrs/s, We intend to carry out medical scientific research in this Centre. It is a study of observation.. This study aims to measure the reliability (variability in recording measurements between two or more operators) of a new method, the ultrasound of a vein in the neck, called the internal jugular vein. This method could be used to better assess congestion (accumulation of fluid in the lung or tissues: vessels and skin) or lack of fluid in the veins, both possible causes of hospitalization.

We are proposing to you to participate in this study because you are hospitalized in the ward and this method allows to understand, together with other elements, the state of \"volemia\" (the amount of liquids present in your veins).

We decided to carry out this study because we would like to verify if the ultrasound of the internal jugular vein is reliable, that is it can be used by several operators without variations in the measurements . This would allow, after further studies, to use it in clinical practice for the management of people who may need fluid infusion or therapies to increase fluid removal.

The study aims to evaluate the reliability (variability in recording measurements between two or more operators) of ultrasound of a vein of the neck, called internal jugular vein In particular we would like to understand if there is a variability in the execution of the ultrasound of the jugular vein between several operators- doctors simultaneously to the same patient. In fact, this method is not currently used in current clinical practice, but if we demonstrate that it is reliable (ie more operators record the same measurements on the same patient , without variations), after further confirmation studies have been conducted , could be used in clinical practice. Its use could, in our view, improve the management of many situations, as it would allow doctors to understand whether the person examined is suffering from \"congestion\", that is, accumulation of water in the lungs and tissues or lack of fluids. This would allow the doctor to take appropriate therapies to reduce congestion or increase fluid.

During the hospitalization, on one occasion, will be submitted to an ultrasound examination of the neck on the right , simultaneously by two or three operators (doctors) . Each operator's examination should take about 10-15 minutes. So the time you spend on it should be 20-30 minutes. The examination will be carried out in bed, in his room with the back tilted 45 degrees and the neck slightly turned to the left.

The necessary treatment and examinations will be carried out and the reason for his admission will be continued.

There is no health risk, as ultrasound is a non-invasive examination based on ultrasound. The only discomfort is to be subjected for about thirty minutes to two or three consecutive examinations. There are no direct benefits to the participants. The study is oriented towards acquiring more scientific knowledge.

02

Conditions studied

  • Hypervolemia
  • Hypovolemia

Browse trials for

Keywords

  • reliability
  • internal jugular vein
  • ultrasound
03

In context

Hypovolemia

133 studies on the registry are indexed under Hypovolemia; 19 are open to participants now.

This study's enrollment of 10 is below the median of 52 across 63 observational studies indexed under Hypovolemia.

Browse Hypovolemia studies →

Lead sponsor

Maggiore Bellaria Hospital, Bologna is the lead sponsor of 9 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

We will include 2 populations:

Patients admitted , for any causes, to the Medicine Department (we will record a group of 6 images that will be used by the sonographers).

Sonographers from Medicine Department

Inclusion criteria

  • patients, admitted to the Medicine Department of Hospital Maggiore in Bologna and eight expert sonographers

Exclusion criteria

Exclusion Criteria:

  • impossibility in providing consent, presence of central venous catheter in the internal jugular vein, thrombosis of the vein
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
10 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Inter-rater reliability of Internal Jugular Vein Ultrasound measures

    We will measure the variability in recording, among 8 sonographers, of 4 Ultrasound measures of Internal Jugular Vein : the antero-posterior diameters, the area, the aspect ratio and the collapsibility index

    Time frame: From enrollment to the end of recording (within 2 months of starting the study)

07

Study locations

1 site
  • Hospital Maggiore
    Bologna, 40125, Italy
08

References and documents

Individual participant data

Plan to share: Yes — I will share the study protocol.

Supporting information: Study protocol

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 19, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06591234
Lead sponsor
Maggiore Bellaria Hospital, Bologna
Responsible party
Nicola Parenti (MD, Maggiore Bellaria Hospital, Bologna) — Principal investigator
First posted
Sep 19, 2024
Start date
Sep 5, 2024
Primary completion
Dec 31, 2024 (estimated)
Completion
Dec 31, 2024 (estimated)
Last update
Sep 19, 2024

Study contacts

Nicola Parenti, MD
principal investigator · Medicina Interna Hospital Maggiore Bologna

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Sep 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion