Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07315178

Creation of a Digital Twin for Predicting the Progression of Patients With Chronic Thoracic Aortic Dissection

Led by Centre Hospitalier Universitaire Dijon · Updated on 2026-01-02

400

Participants Needed

1

Research Sites

309 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Aortic dissection causes a tear in the inner layers of the aorta, leading to the formation of a true and false lumen. There are two types of dissection: type A, which affects the ascending aorta, and type B, which affects the descending aorta. Type A aortic dissection is almost always a surgical emergency and involves replacing the ascending aorta with a prosthesis. After this type of dissection, a residual dissection remains in the descending aorta, known as residual type B dissection, which becomes chronic. This requires increased monitoring by MRI or CT scan, which are currently not effective enough to predict the development of an aneurysm that could lead to aortic rupture requiring surgical intervention. Other factors such as blood flow, the forces and mechanisms regulating blood circulation, the mechanics and histology of the aorta, and blood markers could provide a more reliable prediction of the development of an aneurysm. The creation of a digital twin model incorporating all these factors should enable better patient management.

CONDITIONS

Official Title

Creation of a Digital Twin for Predicting the Progression of Patients With Chronic Thoracic Aortic Dissection

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Person who has given written consent
  • Age > 18 years
  • Patient with type A aortic dissection with surgical indication for replacement
  • Patient with chronic type B aortic dissection, monitored and managed medically, not operated on
Not Eligible

You will not qualify if you...

  • Persons not affiliated with or not covered by a social security scheme
  • Persons subject to legal protection measures (guardianship)
  • Persons subject to judicial protection measures
  • Pregnant women, women in labour or breastfeeding
  • Adults who are incapacitated or unable to give their consent
  • Contraindications to MRI: claustrophobia, non-MRI-compatible metal implants, suspected metal foreign body
  • Severe renal failure (clearance <30ml/min according to Cockroft due to gadolinium injection)
  • Uncontrolled asthma
  • Patients with acute type A aortic dissection who died during or in the post-operative period following surgery to repair the dissection
  • Patients with a known allergy to gadolinium-based contrast agents
  • Patients treated for type B aortic dissection who underwent surgery

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Chu Dijon Bourgogne

Dijon, France, 21000

Actively Recruiting

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Research Team

A

Alain Lalande

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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