Actively Recruiting
Prospective, Post-registration, Interventional, Randomized, in Parallel Groups, Multicenter Eurasian Clinical Study of DERIVO®/DERIVO® Mini Aneurysm Embolization Device, Europe-Asia
Led by Federal State Budgetary Institution, V. A. Almazov Federal North-West Medical Research Centre, of the Ministry of Health · Updated on 2024-05-06
640
Participants Needed
1
Research Sites
258 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Prospective, post-registration, interventional, randomized, in parallel groups, multicenter Eurasian clinical study of DERIVO®/DERIVO® mini Aneurysm Embolization Device, Europe-Asia
CONDITIONS
Official Title
Prospective, Post-registration, Interventional, Randomized, in Parallel Groups, Multicenter Eurasian Clinical Study of DERIVO®/DERIVO® Mini Aneurysm Embolization Device, Europe-Asia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aneurysm location and structure suitable for DERIVO4/DERIVO4 mini flow-diverting stent treatment
- Aneurysm cannot be cured by other endovascular therapies or these therapies have higher complication risks
- Recurrence of aneurysm after previous clipping or embolization with spirals
You will not qualify if you...
- Younger than 18 years
- Pregnant
- Previously implanted stent in a cerebral artery
- Dissection of cerebral or peripheral vessels
- Contraindications to DERIVO4/DERIVO4 mini device including unsuitable aneurysm or vessel structure, and vascular disorders contraindicating endovascular interventions
- Contraindications to antiplatelet or anticoagulant therapy as per medical drug instructions
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
V.A. Almazov Fnmrc
Saint Petersburg, Russia, 197341
Actively Recruiting
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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