Clinical trial Recruiting at 1 site Observational Ages 50 and up Women only

Measuring abdominal aorta diameter in women 50 and older

Official title: Studio Osservazionale Prospettico Multicentrico nazionAle Nel Sesso Femminile peR la valutaziOne Del DIametro Dell'aorTa addominalE - A National, Multicenter, Prospective Observational Study in Females to Assess Abdominal Aortic Diameter

Run by Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico · NCT07487961 · Data updated 2026-11-12

This project will measure abdominal aorta and common iliac artery sizes and collect reproductive and health history from women aged 50 and older to define typical diameters and identify female-specific risk factors for aortic disease.

More Coarctation of Aorta trials

Quick facts

Study typeObservational
Ages50 Years and up
SexWomen only
Enrollment652 (estimated)
SponsorFondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
Academic / other
Locations1 site (Milan)
StatusRecruiting
StartedSeptember 29, 2025
Main results expectedJuly 30, 2027
Study endsJuly 30, 2027
Registry record updatedMarch 27, 2026
Trial IDNCT07487961 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Women aged 50 years or older who can provide informed consent and who have no prior diagnosis of thoracic or abdominal aortic aneurysm and no prior aortic surgery are ideal candidates.

Probably not a fit

Women under 50, those with a prior aortic aneurysm diagnosis or prior open or endovascular aortic surgery, and individuals unable to consent are excluded and unlikely to benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Women aged 50 and older without prior aortic aneurysm or aortic surgery will be enrolled and undergo ultrasound measurement of the abdominal aorta and common iliac arteries using standard perpendicular probe placement with inner-to-inner and outer-to-outer caliper recordings. Measurements will include antero-posterior and lateral diameters and documentation of thrombus or calcification. Investigators will also collect demographic, pathophysiological, and reproductive history data including menarche, pregnancy/infertility, and menopause. The primary goal is to define ultrasound reference diameters in the female population and secondarily to identify sex-specific risk factors for abdominal aortic disease.

Why it matters

Potential benefit: If successful, this work could establish female-specific aortic diameter reference ranges and help identify women at higher risk of aneurysm or rupture, improving screening and treatment timing.

How similar studies have gone: Standard ultrasound measurement techniques are well established, but dedicated studies defining female-specific aortic diameter norms are limited, so this approach addresses a relatively understudied area.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* female sex
* ≥ 50 YO

Exclusion Criteria:

* \< 50 years
* Previous diagnosis of abdominal/thoracic aneurysm disease
* Subjects who have previously undergone surgery (both open and endovascular) on the thoracic and/or abdominal aorta
* Presence of mental disability and/or inability to sign informed consent

Where it's running

  • Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
    Milan, Italy
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.