Clinical trial Recruiting at 6 sites Observational Ages 40 to 90

Creating AI tools to predict vascular disease risk and progression

Official title: Developing Trustworthy Artificial Intelligence (AI)-Driven Tools to Predict Vascular Disease Risk and Progression

Run by Amsterdam UMC, location VUmc · NCT06206369 · Data updated 2026-11-12

This study is trying to create smart computer tools that can predict the risk and progression of vascular diseases like abdominal aortic aneurysm and peripheral arterial disease by looking at medical images and patient history.

Quick facts

Study typeObservational
Ages40 Years to 90 Years
SexAll
Enrollment11000 (estimated)
SponsorAmsterdam UMC, location VUmc
Academic / other
Locations6 sites (Helsinki and 5 other locations)
StatusRecruiting
StartedOctober 31, 2023
Main results expectedMay 1, 2029
Study endsMay 1, 2029
Registry record updatedOctober 5, 2026
Trial IDNCT06206369 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are males and females aged 40-90 with an AAA greater than 3cm or any stage of PAD.

Probably not a fit

Patients with ascending, thoracic, or thoracoabdominal aneurysms will not 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

The VASCULAID-RETRO study aims to develop artificial intelligence algorithms that can predict cardiovascular events and the progression of abdominal aortic aneurysm (AAA) and peripheral arterial disease (PAD). By analyzing data from at least 5000 AAA and 6000 PAD patients, the study will utilize existing cohorts and retrospectively collected data. The AI tools will perform automatic anatomical segmentation and analyses on multimodal imaging, while prediction algorithms will be based on a combination of imaging, medical history, and -omics data. This innovative approach seeks to enhance the understanding of disease progression and risk assessment in vascular conditions.

Why it matters

Potential benefit: If successful, this study could significantly improve the ability to predict cardiovascular events and disease progression in patients with AAA and PAD.

How similar studies have gone: Other studies utilizing AI for predicting vascular disease risk have shown promise, indicating a potential for success in this novel approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria AAA:

* Males and females
* 40-90 years old,
* Infrarenal, juxtarenal, suprarenal, iliac aneurysms (defined as 1.5x its normal diameter), and mycotic aneurysms.
* Starting AAA diameter \>3cm,
* Patients that both have had or did not have interventions or ruptures.

Exclusion Criteria AAA:

* Patients with solely an ascending, thoracic, thoracoabdominal (type 1-3) aneurysm.

Inclusion Criteria PAD:

* Males and females,
* 40-90 years old,
* All PAD patients; all Fontaine stages 1,2,3, and 4.

Exclusion Criteria PAD: None

Where it's running

  • Hospital District of Helsinki and Uusimaa (HUS)
    Helsinki, Finland
    Recruiting
  • Asklepios kliniken hamburg
    Hamburg, Germany
    Recruiting
  • Amsterdam UMC
    Amsterdam, Netherlands
    Recruiting
  • University Hospital Center of São João
    Porto, Portugal
    Recruiting
  • University Clinical Centre of Serbia
    Belgrade, Serbia
    Recruiting
  • Oxford University Hospitals
    Oxford, United Kingdom
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.