Taking peopleNo phase
Unruptured Cerebral Aneurysm: Prediction of Evolution
Key facts
- Who runs it
- Nantes University Hospital
- Where
- Bern, SwitzerlandSee the siteAlso in 2 other countries, 28 sites
- Trial code
- Status
- Recruiting
- People taking part
- 1,000 people, planned
- Started
- 19 Aug 2019
- Expected to end
- 15 Mar 2031
- Type of study
- Observational
- Treatments tested
- Unruptured intracranial aneurysms
- Record updated
- 25 September 2026
Who can take part
- Age
- 18 years and older
- Sex
- Women and men
- Healthy volunteers
- Cannot take part
The registry criteria, word for word
Show all 9 criteriaShow less
Who can take part
- Subject carrying unruptured, asymptomatic and untreated typical IA of bifurcation, measured on conventional imaging (MRI, CTA or DSA) between 3 and 7 mm of larger diameter
- Ability to be followed-up during 3 years decided in consensus multidisciplinary gathering
- Age > 18 years old
Who cannot take part
- A failure to obtain informed consent
- Contraindications for undergoing an MRI scan include : (heart pacemaker, a metallic foreign body (metal sliver) in their eye, or aneurysm clip in their brain, severe claustrophobia)
- A family history of polycystic kidney disease, Ehlers-Danlos syndrome, Marfan's syndrom, fibromuscular dysplasia, or Moya Moya disease
- Contraindications for a gadolinium contrast medium injection (:eGFR below 30 mL/min/1.73 m2, Previous or pre-existing nephrogenic systemic fibrosis, Previous anaphylactic/anaphylactoid reaction to gadolinium containing contrast agent, Acutely deteriorating renal function, Pregnancy and breast-feeding)
- A mycotic, fusiform-shaped, or dissecting IA, an IA in relation with an arteriovenous malformation
- Intra-cavernous UIA because the sinus cavernous that is fulfilled with venous blood precluded a reliable assessment of aneurysmal wall enhancement (AWE)
Where in Switzerland
Also in 2 other countries, 28 sites
- InselHospital BernBern, SwitzerlandContact: Romain BOURCIER, MDNot yet recruiting
About the trial
What the trial wants to find out
The protocol has many assets. A prospective nationwide recruitment allows for the inclusion of a large cohort of patients with UIA. It will combine accurate clinical phenotyping and comprehensive imaging with CAWE screening. Besides, it will enable to exploit metadata and to explore new pathophysiological pathways of interest by crossing clinical, genetic, biological, and imaging information.
Treatments tested
- Unruptured intracranial aneurysms
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Record updated
- 25 September 2026