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Recruiting

NCT Number: NCT06235619

Arch Size Study for Anatomical Variations

The aortic arch with a common origin of the innominate and left carotid artery (CILCA) prevalence in the general population is 13.6%. Its reputation as a benign anatomical variant has been ultimately shattered by further studies that identified the CILCA arch as a potential marker for thoracic aortic disease (TAD) The aim of this work is to report the CT anatomical characteristics of the aortic arch in subjects with or without aneurysms requiring treatment, in 5 major European cardiovascular centers.

Recruiting

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Key information

Age range

0 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

IRCCS San Raffaele Hospital

Milan, Italy, 20132

Location status: Recruiting

Location contact

Germano Melissano, Prof., MD

CONTACT

[email protected]

0226437146

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

all patients with aortic arch CT scan at investigating centers

Exclusion criteria

none

Treatment and study plan

Primary outcomes

  1. difference from baseline of aortic arch anomalies

    Time frame: 30 day

    record of anatomical variations of the aortic arch

Sponsors and collaborators

Lead sponsor

IRCCS San Raffaele

Other

Registry information

Official study title

CT Anatomical Characteristics of the Aortic Arch in Subjects With or Without Aneurysms Requiring Treatment

Important dates

Study start
2024
Primary completion
2025
Study completion
2026
First posted
Feb 1, 2024
Registry last updated
May 2, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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