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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

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Record updated
25 September 2026