New Advanced Vascular Imaging Ultrasound Protocols

NCT ID: NCT06841887

Last Updated: 2025-09-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

60 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-05-09

Study Completion Date

2027-03-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This is a single-center observational study aimed at setting up and testing new ultrasound vascular imaging protocols, conducted exclusively for research purposes. The study will perform US examinations in 60 subjects. The subjects enrolled in the study will be examined the first time and will then provide consent to be examined again in the future if needed.

The primary aim of this study is to set-up and test new advanced US protocol for the arm and cerebral blood vessels

The secondary objectives will be:

* Define ranges of normality/reference values of US-based parameters to be compared with pathological values.
* Evaluate the repeatability and reproducibility of the acquired US measurements.
* Evaluate the correlation between age and the acquired US measurements.
* Evaluate the correlation between gender and the acquired US measurements.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The Medical Imaging Laboratory of Istituto di Ricerche Farmacologiche Mario Negri IRCCS deals with the processing of diagnostic images, allowing quantitative analysis of anatomical structures and organs functions in vivo. The research activities of the group are focused on: i) developing novel techniques to segment and quantify anatomical structures and pathological lesions in response to specific clinical needs; ii) identifying and validating novel imaging biomarkers, iii) investigating novel morphologic and hemodynamic changes in different vascular districts and the role of hemodynamics in vascular disease onset and progression. Besides these activities, increasing efforts have recently been devoted to exploring the potential of novel imaging solutions and in setting up new non-invasive imaging protocols. These protocols have been primarily developed for the kidney and renal arteries, the cerebral vasculature, and the arteriovenous fistula used in hemodialysis, which are the main focus of the Medical Imaging Lab's activities. Specifically, in 2024 Istituto di Ricerche Farmacologiche Mario Negri IRCCS purchased the new ultrasound (US) machine Resona 9, within the ANTHEM project (ID: NCT05996731). Resona 9 is the top-of-the-line model among Mindray's ultrasound machines. It combines advanced features to deliver exceptional image quality with a suite of artificial intelligence-enhanced technologies designed to help clinicians improve reproducibility and optimize productivity. Specifically related to our research focus, the Resona 9 incorporates novel advanced functionalities to accurately measure vascular wall thickness and stiffness. Moreover, the VFlow technique enables the visualization of complex blood flow features. Our Resona 9 is also equipped with the PIUR tUS device, which transforms the US system into a tomographic 3D solution device. This allows the acquisition of a stack of images of the blood vessels and the reconstruction of 3D virtual models, with big advantages in terms of costs and velocity of the acquisition as compared to conventional magnetic resonance imaging.

To take full advantage of all these US-based techniques and make the most out of Resona 9 tools on patients with renal and cerebral pathologies, there is an urgent need of setting up dedicated US protocols and testing. This step will also allow collecting ranges of normality/reference values of image-based parameters, to be later used to compare with corresponding specific parameters acquired in patients.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Renal Diseases Cerebral Disorder

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Males, age group 1

Male subjects aged 18-40 years

US acquisitions

Intervention Type DIAGNOSTIC_TEST

US acquisition from two anatomical regions i.e., the non-dominant arm and the neck.

Males, age group 2

Male subjects aged 41-55 years

US acquisitions

Intervention Type DIAGNOSTIC_TEST

US acquisition from two anatomical regions i.e., the non-dominant arm and the neck.

Males, age group 3

Male subjects aged 56-75 years

US acquisitions

Intervention Type DIAGNOSTIC_TEST

US acquisition from two anatomical regions i.e., the non-dominant arm and the neck.

Female, age group 1

Female subjects aged 18-40 years

US acquisitions

Intervention Type DIAGNOSTIC_TEST

US acquisition from two anatomical regions i.e., the non-dominant arm and the neck.

Females, age group 2

Female subjects aged 41-55 years

US acquisitions

Intervention Type DIAGNOSTIC_TEST

US acquisition from two anatomical regions i.e., the non-dominant arm and the neck.

Females, age group 3

Female subjects aged 56-75 years

US acquisitions

Intervention Type DIAGNOSTIC_TEST

US acquisition from two anatomical regions i.e., the non-dominant arm and the neck.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

US acquisitions

US acquisition from two anatomical regions i.e., the non-dominant arm and the neck.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Provision of informed consent prior to any study specific procedures
* Female and/or male aged between 18 and 75 years
* No previous history of kidney or cerebral disease and no pathologies that might have affected the vascular system

Exclusion Criteria

* Previous history of kidney or cerebral disease or pathologies that might have affected the vascular system
* Legal incapacity, limited legal capacity, intellectual disability, uncooperative attitude or any other evidence that the subject will not be able to understand the study aims and procedures
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Mario Negri Institute for Pharmacological Research

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Giuseppe Remuzzi, M.D.

Role: STUDY_DIRECTOR

Istituto Di Ricerche Farmacologiche Mario Negri

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Clinical Research Centre for Rare Diseases Aldo e Cele Daccò

Ranica, BG, Italy

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Italy

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Michela Bozzetto, Ph.D.

Role: CONTACT

+39 035 4535 381

Luca Soliveri

Role: CONTACT

+39 035 4535 381

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Matias Trillini, M.D.

Role: primary

+39 035 4535 411

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

RESONA-SETTING

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Sympathetic Mapping/ Ablation of Renal Nerves Trial
NCT02761811 ACTIVE_NOT_RECRUITING NA