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RecruitingNCT06689410bCANUpdated Sep 2, 2026

Multimodal Biocollection Linked to the French Register of Intracranial Aneurysms

An interventional study of blood or saliva sample in Aneurysm, Brain Aneurysm and Congenital Disease, sponsored by Nantes University Hospital. Recruiting at 26 sites in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-02.

Primary conditionIntracranial AneurysmRegistry: AneurysmReclassifiedWhy we changed it
Registry
Aneurysm — the first condition term the registry derived for this study.
ClinicalTrials.gg
Intracranial Aneurysm
Why
  1. The study's listed conditions name Intracranial Aneurysm, a narrower term within Aneurysm.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Nantes University Hospital · Not applicable, Interventional, and Other

From the registry’s dates

  • Started Mar 2025; still recruiting 1 year 7 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
1,100
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study 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.

Read the detailed description

The main objective of bCAN study is to build a predictive model of intracranial aneurysm phenotypes through the combination of information on genetic mutations, imaging findings and ICA rupture characteristics.

The secondary objectives of the bCAN study are (i) to study morphological characterization of ICA and vascular bifurcations, (ii) to deepen knowledge of genotype/clinical and biological phenotype relationships according to the genes identified in the different families, (iii) to research and validate the relationships between genotypes and phenotypes (including rupture) of ICA in a large population of sporadic ICA cases.

02

Conditions studied

  • Aneurysm
  • Brain Aneurysm
  • Congenital Disease

Keywords

  • intracranial aneurysm
  • phenotype
  • genetics
  • imaging
  • multimodal data
03

In context

Intracranial Aneurysm Reclassified

418 studies on the registry are indexed under Intracranial Aneurysm; 119 are open to participants now.

This study's planned enrollment of 1,100 is above the median of 100 across 207 interventional studies indexed under Intracranial Aneurysm.

Browse Intracranial Aneurysm studies →

Lead sponsor

Nantes University Hospital is the lead sponsor of 839 studies on the registry; 195 are open to participants now.

Compared within Intracranial Aneurysm, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Aneurysm. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 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

Inclusion criteria for index and related cases (familial forms) of intracranial aneurysms (ICA):

  • Index case: Any adult patient consulting for a definite and typical bifurcation ICA presenting at least one other case with ICA related (child, parent, brother, sister) detected by MRI with at least one Time of Flight (TOF) sequence.
  • Family relatives: children, parents, brothers, sisters, of legal age, of patients with a family history of definite, typical bifurcation AIC (≥ 4 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

Exclusion criteria

Exclusion Criteria:

  • Syndromic diagnosis known to cause ICA: Marfan syndrome, OSA with SMAD 3, Elhers Danlos syndrome type II and IV, Autosomal Dominant Cystic Fibrosis, Moya-Moya syndrome
  • AIC with : Dissecting or fusiform, Associated with arteriovenous malformation, Blister-like, Mycotic
  • Cerebral white matter pathology detected on MRI evoking : Col4a1 mutation
  • Patient under guardianship or conservatorship
  • Person under court protection
  • to an MRI scan
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
1,100 participants (estimated)

Study arms

  • Other
    ICA cases

    Any adult patient consulting for a definite and typical bifurcation AIC authenticated on MRI and/or cerebral arteriography

    Other: blood or saliva sample

Interventions

  • Otherblood or saliva sample

    Collection of blood or saliva

06

What researchers measure

Primary outcomes

  1. Performance of a predictive model allowing the classification of ICA subphenotypes

    The performance of a predictive model allowing the classification of ICA subphenotypes will be analysed through the study of genetic results, quantitative features extracted from imaging and clinical data on rupture

    Time frame: 36 months

Secondary outcomes

  1. Characterization of arterial bifurcations

    Quantitative morphological measurements of arterial bifurcations assessed using image processing tools enabling automatic characterization (artery diameters (in mm); artery cross-sections (in mm²); angles separating arteries (in degrees)

    Time frame: 36 months

  2. Characterization of aneurysmal sacs

    Quantitative morphological measurements of aneurysmal sacs assessed using image processing tools enabling automatic characterization (volume (in mm³); external surface area of the envelope (mm²); neck area (mm²))

    Time frame: 36 months

  3. Screening of genetic mutations

    Presence of genetic mutations in patients with intracranial aneurysms compared with a reference population, but also in a familial context. Genetic variations will be studied by whole exome sequencing

    Time frame: 36 months

  4. Correlation between genotypes and phenotypes

    Correlations between genetic mutations and the different clinical and biological phenotypes described in patients with sporadic ICA

    Time frame: 36 months

07

Study locations

10 of 26 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Mar 2025 (actual). Primary completion is estimated for Mar 2027, 24 months after the start.

Of 56 non-industry interventional studies with no phase under Intracranial Aneurysm, half reached primary completion within 59 months of starting (the median), counting those still running; a quarter within 30 and three quarters within 134. This study's planned 24 months is below that.

Counting every sponsor, half of 104 studies reached it within 39 months; a quarter within 22 and three quarters within 69.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 31, 2024
First posted
Nov 14, 2024
StartActual
Mar 25, 2025
Primary completionEst.
Mar 25, 2027
CompletionEst.
Mar 25, 2027
Last update
Sep 2, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06689410
Collaborators
Federation of Medical Specialties
Responsible party
Sponsor
First posted
Nov 14, 2024
Start date
Mar 25, 2025
Primary completion
Mar 25, 2027 (estimated)
Completion
Mar 25, 2027 (estimated)
Last update
Sep 2, 2026

Study contacts

Romain BOURCIER, MD
Contact
romain.bourcier@chu-nantes.fr
33240165608
Romain BOURCIER, MD
principal investigator · Nantes University Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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