@neurIST : Intregrated Biomedical Informatics for the Management of Cerebral Aneurysms (NCT05526352)
@neurIST : Informatique biomédicale intégrée Pour la Gestion Des anévrismes cérébraux
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: University of California — San Francisco, California
Age range: 18 Years
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (22 Sites)
- University of California — San Francisco, California
- University of Cincinnati College of Medicine — Cincinnati, Ohio
- University of Virginia — Virginia Beach, Virginia
- Montreal Neurological Institute and Hospital, McGill University — Montreal,
- Helsinki University Central Hospital — Helsinki,
- Kuopio University Hospital — Kuopio,
- ICAN — Nantes,
- Department of Neurosurgery, Klinikum rechts der Isar, Technical University Munich — Munich,
- University of Pecs — Pécs,
- Erasmus Medical Center — Rotterdam,
- University Medical Center Utrecht — Utrecht,
- Jagiellonian University Medical College — Krakow,
- Barcelona Hospital General de Cataluna — Barcelona,
- Hospital Clinic Barcelona — Barcelona,
- IMIM - Hospital del Mar — Barcelona,
- Neurochirurgie / Hôpitaux Universitaire de Genève — Geneva,
- University Hospital of Lausanne (CHUV), CoLaus Datacenter — Lausanne,
- Department of Neurosurgery, Cantonal Hospital St. Gallen — Sankt Gallen,
- Klinik Hirslanded — Zurich,
- University College London — London,
- Radcliffe Infirmary — Oxford,
- Royal Hallamshire Hospital — Sheffield,
📞 Contact the Study Coordinator
Phone: +41 58 934 54 44
Email: hirc@zhaw.ch
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Intracranial Aneurysm
- SEAL™IT: Saccular Endovascular Aneurysm Lattice System Interventional Pivotal Trial — Arlington Heights, Illinois
- INSPIRE Pipeline™ Shield Post Approval Study — Birmingham, Alabama
- MicroVention, Inc. Flow Re-Direction Endoluminal Device X (FRED™ X™) Post-Approval Study — Hollywood, Florida
- Intravascular Neuro OCT Imaging System for Aneurysm Treatment Evaluation — Jacksonville, Florida
- Brain Low-risk Aneurysm Stereotactic Radiosurgical Trial — Sherbrooke, Quebec
- NV PSR INSPIRE-A Pipeline™ Vantage Post Approval Study — Jacksonville, Florida
Explore by condition: All Intracranial Aneurysm clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.