Multimodal Biocollection Linked to the French Register of Intracranial Aneurysms

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Any adult patient consulting for a definite and typical bifurcation AIC 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 ICA presenting at least one other case with ICA related to the 1st or 2nd degree (child, parent, brother, sister) detected by MRI with at least one Time of Flight (TOF) sequence.

• Family relatives: All 1st- and 2nd-degree relatives (children, parents, brothers, sisters), of legal age, of patients with a family history of definite, typical bifurcation AIC (≥ 2 affected), Screening to be performed using MRI with at least a Time of Flight (TOF) sequence.

• Written consent to participate in the study

• Patient and relatives covered by a social security plan

Locations
Other Locations
France
Nantes University Hospital
RECRUITING
Nantes
Contact Information
Primary
Romain BOURCIER, MD
romain.bourcier@chu-nantes.fr
33240165608
Time Frame
Start Date: 2025-03-25
Estimated Completion Date: 2028-04-01
Participants
Target number of participants: 1100
Treatments
Other: ICA cases
Any adult patient consulting for a definite and typical bifurcation AIC authenticated on MRI and/or cerebral arteriography
Related Therapeutic Areas
Sponsors
Leads: Nantes University Hospital
Collaborators: Inserm UMR1087, CNRS UMR6291, Federation of Medical Specialties

This content was sourced from clinicaltrials.gov