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Multimodal Biocollection Linked to the French Register of Intracranial Aneurysms

Study acronym: bCAN
StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Site details revised at 8 of 26 sitesv5
  2. Trial sites expanded: 2 → 26 locationsv4
  3. Study sites: 1 to 2
    • Study completion date: Apr 1, 2028 to Mar 25, 2027
    • Eligibility criteria shortened, about 11 words
    • Collaborators: 2 to 1
    v3
  4. Trial status: Not Yet Recruiting to Recruitingv2 Show 4 more changesShow less
    • Study sites: 0 to 1
    • Primary completion date: Jan 1, 2027 to Mar 25, 2027
    • Study completion date: Jan 1, 2028 to Apr 1, 2028
    • Start date changed from estimate of Jan 1, 2025 to Mar 25, 2025
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT06689410
Lead Sponsor Nantes University Hospital
Collaborators: Federation of Medical Specialties
Conditions
(from sponsor)		 Aneurysm, Brain Aneurysm, Congenital Disease
Related terms Aneurysm, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Intracranial Aneurysm
Enrollment 1,100 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov