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Study identifier: NCT07487961 Synced from ClinicalTrials.gov · July 29, 2026
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Assess Abdominal Aortic Diameter in Females

Condition: Aorta Disease · Aorta Aneurysm  ·  Sponsor: Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

PhaseN/A
Planned participants652
Who can joinFemale, 50 Years to no upper limit
Healthy volunteersYes

About this study

Female subjects aged 50 years or older will be enrolled. Biometric data (measurements) of the aorta and iliac vessels, demographic data, pathophysiological history, and data relating to menarche, pregnancy/infertility, and menopause will be collected. The aortic diameter measurement protocol will follow standard clinical practice. Measurements will be performed by placing the probe on an axis perpendicular to the aortic axis, manually positioning the calipers in the antero-posterior and lateral-lateral directions, recording both the outer-to-outer (OTO) and inner-to-inner (ITI) diameters. Additionally, the presence of thrombus and/or calcifications and the outer-to-outer (OTO) measurement of the common iliac arteries will be detected. Primary objective: Definition of the ultrasound diameter of the abdominal aorta in the female population. Secondary objective: Identification of any sex-specific risk factors associated with abdominal aortic disease (aneurysm) in the female population. Secondary objective: Identification of any sex-specific risk factors associated with abdominal aortic disease (atherosclerosis) in the female population.

This description comes directly from the study's public registry record.

Talk to the study team

CHIARA LOMAZZI, MD  ·  +390255036670  ·  chiara.lomazzi@policlinico.mi.it

Always discuss trial participation with your own doctor first.

Locations (1)

Fondazione IRCCS Ca' Granda Ospedale Maggiore PoliclinicoMilan, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT07487961