Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT05526352

@neurIST : Intregrated Biomedical Informatics for the Management of Cerebral Aneurysms

Led by University Hospital, Geneva · Updated on 2026-01-16

20000

Participants Needed

22

Research Sites

1291 weeks

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

The primary aim of the SwissNeuroFoundation AneurysmDataBase Project is to implement information technology based tools to create and use a holistic reference database specific to intracranial aneurysms (IA). The SwissNeuroFoundation AneurysmDataBase are concerned with generating the data with which to populate this database. The purpose for populating the database are to: * Screen for and evaluate markers of risk for intracranial aneurysm formation and aneurysm rupture. Are considered as markers the following: genetics factors, microbiota, environmental factors, congenital factors (ie: cerebrovascular anatomical variants), transcriptomics signature, proteomics signature,shape characteristics, haemodynamics characteristics. * Screen for and evaluate prognostic factors of outcome regarding different management strategies including watchful observation, microsurgical treatment, endovascular treatment or any combination thereof. * Implement and evaluate patient-specific management protocols integrating all available information. * Evaluate the impact of the database and use of tools to improve care, reduce costs, support knowledge discovery and promote new industrial developments.

CONDITIONS

Official Title

@neurIST : Intregrated Biomedical Informatics for the Management of Cerebral Aneurysms

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Able to provide consent or have a legally authorized person provide consent according to local laws and ethics
  • Patients must have an angiographically confirmed intracranial aneurysm (MRA, CTA, or DSA accepted)
  • Verification of subarachnoid hemorrhage (SAH) requires CT scan or lumbar puncture confirmation
Not Eligible

You will not qualify if you...

  • Failure to provide clinical data
  • Refusal to give informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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

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Research Team

S

Sven Hirsch, Dr

CONTACT

P

Philippe Bijlenga, PD MD PhD

CONTACT

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

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