Multimodal Biocollection Linked to the French Register of Intracranial Aneurysms
Ennek a vizsgálatnak nincs helyszíne itt: Egyesült Államok.
Egy országban van helyszíne. Válassz országot, hogy lásd a helyszíneket.
Kérdések a vizsgálat csapatának
- Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
- Megtérítik az utazási költséget?
- Megtarthatom a saját orvosomat?
- Mi történik, ha ki akarok lépni?
Contact the study team: see the registry record → Contacts and Locations
Oldal nyomtatása az orvosomnakA vizsgálat adatai
- Ki végzi
- Nantes University Hospital
- Azonosító
- NCT06689410
- A regiszteradat frissítve
- 2026. szeptember 2.
- Eredeti leírás
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).A teljes eredeti leírásKevesebb
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.
Bevonási feltételek: 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 (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.
Kizáró feltételek: 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; Contraindication to an MRI scan.