Actively Recruiting
Microvention AnEurysm & STroke Real-life Data cOllection
Led by Microvention-Terumo, Inc. · Updated on 2026-02-09
1000
Participants Needed
1
Research Sites
286 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The MAESTRO registry is a post-market, single-arm, non-interventional, multicenter registry
CONDITIONS
Official Title
Microvention AnEurysm & STroke Real-life Data cOllection
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient or authorized person has been informed and consents to data collection according to local regulations
- For Cohort 1, patient treated for ruptured or unruptured intracranial aneurysm with a Microvention implant device as primary treatment decided outside this study
- For Cohort 2, patient treated with a Microvention mechanical thrombectomy device as first-line treatment decided outside this study
You will not qualify if you...
- Patient is or is expected to be unreachable for follow-up
- Patient is participating or plans to participate in another study that changes the treatment site practice
- Patient is already participating in the MAESTRO study for the same condition
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Álvaro Cunqueiro Hospital - University Hospital Complex of Vigo, Department of Radiology
Vigo, Pontevedra, Spain, 36312
Actively Recruiting
Research Team
C
Clinical Team
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
2
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