Actively Recruiting
NEUROvascular NAVigation With Remotely Controlled Deflectable Guidewire, Study I (NeuroNAV Study I)
Led by Artiria Medical · Updated on 2026-01-21
30
Participants Needed
1
Research Sites
76 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of the study is to confirm the safe and successful use of the SmartGUIDE guidewire, when used in neuro interventions. The performance of the SmartGUIDE guidewire in terms of safe and successful navigation within the neurovasculature will be compared to standard of care guidewire on the market.
CONDITIONS
Official Title
NEUROvascular NAVigation With Remotely Controlled Deflectable Guidewire, Study I (NeuroNAV Study I)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Over 18 years of age
- Signed informed consent from the patient
- Confirmed cerebral unruptured aneurysm treatable by transcatheter approach
You will not qualify if you...
- Pregnancy or breastfeeding
- Known vascular fragility disorder with risk of injury (e.g., Ehlers-Danlos syndrome)
- Prior vascular stenosis, dissection, or injury in vessels to be used during the procedure
- Recent heart attack or uncontrolled irregular heartbeat
- Uncontrolled electrolyte imbalance
- Bleeding disorder preventing use of antiplatelet or anticoagulant therapy
- Known allergy to intravascular contrast material not manageable with pre-medication
- Known allergy to Nickel
- Currently enrolled in another investigational device or drug study that affects this study's results
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Centre Hospitalier Universitaire - CHU Limoges
Limoges, France, 87042
Actively Recruiting
Research Team
G
Guillaume Petit-Pierre, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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