Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06689410

Multimodal Biocollection Linked to the French Register of Intracranial Aneurysms

Led by Nantes University Hospital · Updated on 2026-05-05

1100

Participants Needed

2

Research Sites

104 weeks

Total Duration

On this page

Sponsors

N

Nantes University Hospital

Lead Sponsor

F

Federation of Medical Specialties

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of the bCAN study is to create a prospective collection of multimodal data and human samples, linked to the French Intracranial Aneurysm Registry (FRAN). The aim of bCAN is to enable risk stratification of ruptured ICAs by redefining "intracranial aneurysm disease". The description of genotypically and phenotypically specific subgroups of cases will pave the way for improved patient management based on new diagnostic/prognostic strategies among AIC carriers, either in a familial context, or at the level of the general population.

CONDITIONS

Official Title

Multimodal Biocollection Linked to the French Register of Intracranial Aneurysms

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Any adult patient consulting for a definite and typical bifurcation intracranial aneurysm authenticated on MRI and/or cerebral arteriography
  • Aneurysm discovered less than a year ago, with initial imaging (MRI and/or CTA and DSA) available
  • Written consent obtained for study participation
  • Patient covered by a social security plan
  • Index case: Any adult patient consulting for a definite and typical bifurcation intracranial aneurysm presenting at least one other related case detected by MRI with at least one Time of Flight (TOF) sequence
  • Family relatives: children, parents, brothers, sisters, of legal age, with a family history of definite, typical bifurcation intracranial aneurysm (four or more affected), screening by MRI with at least a TOF sequence
  • Written consent to participate in the study
  • Patient and relatives covered by a social security plan
Not Eligible

You will not qualify if you...

  • Syndromic diagnoses known to cause intracranial aneurysms: Marfan syndrome, OSA with SMAD 3, Ehlers-Danlos syndrome type II and IV, Autosomal Dominant Cystic Fibrosis, Moya-Moya syndrome
  • Aneurysms that are dissecting, fusiform, associated with arteriovenous malformation, blister-like, or mycotic
  • Cerebral white matter pathology on MRI suggesting Col4a1 mutation
  • Patient under guardianship or conservatorship
  • Person under court protection
  • Contraindication to an MRI scan

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Nantes University Hospital

Nantes, Loire-Atlantique, France, 44093

Actively Recruiting

2

CHU Clermont-Ferrand

Clermont-Ferrand, France, 63000

Actively Recruiting

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Research Team

R

Romain BOURCIER, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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