Actively Recruiting
European, Multi-center, Exploratory Trial to Assess WEB Versus Other Endovascular Treatment in Ruptured Aneurysms.
Led by Microvention-Terumo, Inc. · Updated on 2024-12-18
80
Participants Needed
1
Research Sites
138 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Comparison of efficacy and safety between WEB and other endovascular techniques
CONDITIONS
Official Title
European, Multi-center, Exploratory Trial to Assess WEB Versus Other Endovascular Treatment in Ruptured Aneurysms.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient is above 18 years of age at the time of consent
- Patient has an identified acutely ruptured intracranial aneurysm requiring endovascular treatment within the last 30 days, confirmed by CT, MRI, or lumbar puncture
- Aneurysm dome diameter is 10mm or less and suitable for treatment by WEB devices and at least one other endovascular treatment device
- Aneurysm is located on the anterior communicating artery complex segment, internal carotid artery terminus, anterior cerebral artery, middle cerebral artery, basilar apex, posterior communicating artery, or pericallosal artery
- Patient is neurologically stable with a Hunt & Hess score of I to III
- Patient or legally authorized representative has provided written informed consent
You will not qualify if you...
- Aneurysm is unsuitable for treatment with WEB devices and/or other available endovascular techniques
- Patient has a blister-like or dissecting aneurysm
- Patient has more than one aneurysm requiring treatment within 30 days of the target aneurysm treatment
- Patient has multiple aneurysms and the ruptured aneurysm cannot be identified
- Patient has a pre-morbid modified Rankin Scale score greater than 2
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CHU Reims
Reims, France
Actively Recruiting
Research Team
C
Clinical Department
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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