Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
60 participants
OBSERVATIONAL
2025-05-09
2027-03-31
Brief Summary
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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.
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Detailed Description
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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
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Males, age group 1
Male subjects aged 18-40 years
US acquisitions
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
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
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
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
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
US acquisition from two anatomical regions i.e., the non-dominant arm and the neck.
Interventions
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US acquisitions
US acquisition from two anatomical regions i.e., the non-dominant arm and the neck.
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
18 Years
75 Years
ALL
Yes
Sponsors
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Mario Negri Institute for Pharmacological Research
OTHER
Responsible Party
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Principal Investigators
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Giuseppe Remuzzi, M.D.
Role: STUDY_DIRECTOR
Istituto Di Ricerche Farmacologiche Mario Negri
Locations
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Clinical Research Centre for Rare Diseases Aldo e Cele Daccò
Ranica, BG, Italy
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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RESONA-SETTING
Identifier Type: -
Identifier Source: org_study_id
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