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Recruiting NCT07666451

Assessment of Cardiac and Carotid Ultrasound Measurements in a Cohort of Healthy Children in Italy

Observational Cardiovascular Imaging Echocardiography Carotid Intima-Media Thickness

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Cardiovascular Imaging, Echocardiography, Carotid Intima-Media Thickness. Basic parameters: 0 years — 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This observational ambispective cohort study aims to establish reference values for cardiac structure and function, coronary artery dimensions, and carotid intima-media thickness (cIMT) in a healthy pediatric population living in Italy. Healthy children aged 0-18 years undergoing cardiologic evaluation will be enrolled. Echocardiographic and carotid ultrasound parameters will be collected together with anthropometric and demographic data. The study includes both retrospective and prospective cohorts.

Primary outcome measures

  • Distribution of echocardiographic and carotid ultrasound measurements [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

Age between 0 and 18 years (inclusive) Availability of demographic and anthropometric data Negative past and recent medical history for chronic or acute diseases Adequate quality of echocardiographic evaluation Written informed consent obtained from parent/legal guardian and assent from the minor when applicable

Exclusion criteria

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Italy · 1 center
  • IRCCS Azienda Ospedaliero - Universitaria di Bologna, U.O. Pediatria — Bologna

Identifiers

NCT: NCT07666451 · NORMECO

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗