Actively Recruiting
A National, Multicenter, Prospective Observational Study in Females to Assess Abdominal Aortic Diameter
Led by Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico · Updated on 2026-03-27
652
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to study abdominal aortic diameter specifically in females aged 50 years or older. It evaluates biometric data of the aorta and iliac vessels along with demographic and health history related to reproductive factors such as menarche, pregnancy, infertility, and menopause. The study focuses on understanding the ultrasound measurements of the abdominal aorta and identifying female-specific risk factors for abdominal aortic diseases including aneurysms and atherosclerosis. Measurements of the aorta will be done using ultrasound by placing the probe perpendicular to the aortic axis and recording diameters in both antero-posterior and lateral directions. Both inner-to-inner and outer-to-outer diameters of the infrarenal aortic segment will be measured, along with assessments for the presence of thrombus and calcifications, and measurements of the common iliac arteries. The study follows standard clinical measurement protocols. Participants will provide biometric data and health history related to cardiovascular and reproductive health. Researchers will analyze ultrasound images and collected data to define typical abdominal aortic diameters in women and explore risk factors linked to aortic disease. The main measurement outcome is the ultrasound diameter of the infrarenal aortic segment. This observational study includes safety monitoring and will continue until July 2027, with the total participation duration varying by individual.
CONDITIONS
Brief Title
Assess Abdominal Aortic Diameter in Females
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female sex
- Age 50 years or older
You will not qualify if you...
- Younger than 50 years
- Previous diagnosis of abdominal or thoracic aneurysm disease
- Prior surgery on the thoracic and/or abdominal aorta
- Presence of mental disability or inability to sign informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 1 day
Participants undergo ultrasound measurement of the abdominal aorta and provide medical history information for assessment of aortic characteristics.
1 visit (in-person)
Duration - Up to 5 years
Participants are observed over time to understand the relationship between abdominal aortic measurements and cardiovascular health in females.
Trial Site Locations
Total: 1 location
1
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
Milan, Italy
Actively Recruiting
Research Team
C
CHIARA LOMAZZI, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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