Actively Recruiting
@neurIST : Integrated Biomedical Informatics for the Management of Cerebral Aneurysms
Led by University Hospital, Geneva · Updated on 2026-01-16
20000
Participants Needed
22
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University Hospital, Geneva
Lead Sponsor
U
University of Geneva, Switzerland
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are working to create and use a comprehensive database focused on intracranial aneurysms (IA). This project collects and studies clinical history, imaging data, biological samples, and other information to understand factors linked to the formation and rupture of aneurysms. They aim to identify genetic, environmental, and anatomical markers, as well as evaluate outcomes from different treatment strategies and improve patient care protocols. Participants include patients with diagnosed aneurysms, both ruptured and unruptured, family members of affected individuals, and healthy volunteers. Data collected involves detailed clinical records, imaging scans like MRI angiography and CT angiography, and various biological samples such as blood, cerebrospinal fluid, saliva, and stool. Consent covers access to medical records, use of biological samples, and potential future research uses including genetic analyses. During the study, participants provide health and lifestyle information, imaging data, and biological samples. Researchers will monitor multiple long-term outcomes including disease progression, life expectancy, quality of life, neurological and cognitive status, and treatment effects over periods up to 20 years. Data confidentiality is maintained, and participants can withdraw at any time without affecting their medical care. The study aims to validate disease models and support advances in aneurysm management and research.
CONDITIONS
Brief Title
@neurIST : Intregrated Biomedical Informatics for the Management of Cerebral Aneurysms
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Able to provide informed consent or have a legal representative authorized to consent
- Patients must have an angiographically confirmed intracranial aneurysm (using MRA, CTA, or DSA)
- Consent to participate as a patient, family member, or healthy volunteer
You will not qualify if you...
- Failure to provide clinical data
- Refusal to provide informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Initial data collection at enrollment
Participants provide clinical history, imaging data, and biological samples to be entered into the SwissNeuroFoundation AneurysmDataBase. This includes demographic information, medical history, family tree, signs and symptoms, imaging analysis, and treatment information.
1 baseline visit (in-person)
Duration - Up to 20 years
Participants' clinical and imaging data, as well as biological samples, are collected and monitored over time to assess disease progression, aneurysm status, and various health outcomes.
Periodic visits depending on clinical need and data updates
Trial Site Locations
Total: 22 locations
1
University of California
San Francisco, California, United States
Actively Recruiting
2
University of Cincinnati College of Medicine
Cincinnati, Ohio, United States
Actively Recruiting
3
University of Virginia
Virginia Beach, Virginia, United States
Actively Recruiting
4
Montreal Neurological Institute and Hospital, McGill University
Montreal, Canada
Actively Recruiting
5
Helsinki University Central Hospital
Helsinki, Finland
Actively Recruiting
6
Kuopio University Hospital
Kuopio, Finland
Actively Recruiting
7
ICAN
Nantes, France
Actively Recruiting
8
Department of Neurosurgery, Klinikum rechts der Isar, Technical University Munich
Munich, Germany
Actively Recruiting
9
University of Pecs
Pécs, Hungary
Completed
10
Erasmus Medical Center
Rotterdam, Netherlands
Completed
11
University Medical Center Utrecht
Utrecht, Netherlands
Actively Recruiting
12
Jagiellonian University Medical College
Krakow, Poland
Actively Recruiting
13
Barcelona Hospital General de Cataluna
Barcelona, Spain
Completed
14
Hospital Clinic Barcelona
Barcelona, Spain
Completed
15
IMIM - Hospital del Mar
Barcelona, Spain
Actively Recruiting
16
Neurochirurgie / Hôpitaux Universitaire de Genève
Geneva, Switzerland, 1211
Actively Recruiting
17
University Hospital of Lausanne (CHUV), CoLaus Datacenter
Lausanne, Switzerland, 1011
Actively Recruiting
18
Department of Neurosurgery, Cantonal Hospital St. Gallen
Sankt Gallen, Switzerland
Actively Recruiting
19
Klinik Hirslanded
Zurich, Switzerland, 8008
Not Yet Recruiting
20
University College London
London, United Kingdom
Actively Recruiting
21
Radcliffe Infirmary
Oxford, United Kingdom
Completed
22
Royal Hallamshire Hospital
Sheffield, United Kingdom
Completed
Research Team
S
Sven Hirsch, Dr
P
Philippe Bijlenga, PD MD PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
4