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Determination of the Aneurysm Vulnerability Index by Stimulation and Medical Imaging

Determination of the Aneurysm Vulnerability Index by Stimulation and Medical Imaging

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05189041
Acronym
ANEUVISM
Enrollment
45
Registered
2022-01-12
Start date
2014-06-30
Completion date
2017-12-31
Last updated
2022-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aneurysm

Keywords

aneurysm

Brief summary

Stroke is the leading cause of disability in France with 130,000 cases per year, 20% of strokes being hemorrhagic, with a majority of intracranial aneurysm rupture (80%). Each year, 6000 meningeal hemorrhages (MHA) caused by cerebral aneurysm rupture are reported in France: 40% of patients die within the first month and 30% are left with severe and permanent disability. Intracranial aneurysms are present in 2 to 6% of the population and only about 0.5% of them will rupture. Given the human and economic costs associated with this disease, systematic medical screening for intracranial aneurysms could be useful. However, the operative risk of endovascular treatment remains non-zero (around 1%) and could be proposed only to a selected population of aneurysms at risk of rupture. The absence of diagnostic criteria for aneurysmal vulnerability does not allow for the moment to consider screening for this disease, which continues to strike without warning a young and active population. Nevertheless, access to brain imaging allows the detection of an increasing number of intracranial aneurysms. The question of preventive treatment then arises and is still a difficult point discussed by neurosurgeons / neurointerventionists based on general epidemiological data difficult to apply to an individual.

Interventions

OTHERAneurysmal pulsation in functional MRI

Quantify the aneurysmal pulsation in functional MRI on the patient with Ruptured Cerebral Aneurysm

Sponsors

University Hospital, Montpellier
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Age limits to \> 18 years * Collection of the informed consent (patient or legal representant) * Affiliation or recipient with the mode of social security \- Groupe anévrysme rompu * Patient porteur d'un anévrysme rompu \- Groupe anévrysme non rompu * Patient porteur d'un anévrysme non rompu

Exclusion criteria

* Subject presenting contraindications in MRI (Ferromagnetic foreign bodies, pace-maker …) * Claustrophobia * Women pregnant or Breast-feeding * Patient participating in an other study * Patient have participated in a study in the 3 months before the inclusion * In period of exclusion relative to another protocol * Person with majority age protected by the law (supervision or trusteeship). * Patient not reading the french language * Patient or representant for whom it impossible to give accurate informations

Design outcomes

Primary

MeasureTime frameDescription
Quantify the aneurysmal pulsation in functional MRI1 dayQuantify the aneurysmal pulsation in functional MRI on the patient with Ruptured Cerebral Aneurysm or Non ruptured Aneurysm

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026