NEUROvascular NAVigation With Remotely Controlled Deflectable Guidewire, Study I (NeuroNAV Study I)
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Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorTrial details
- Who runs it
- Artiria Medical
- Trial code
- NCT06972953
- Record updated
- 21 January 2026
- Original description
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.Read full original descriptionShow less
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.
Inclusion: >18 years of age; Informed consent signed by the patient; Confirmed cerebral unruptured aneurysm treatable via transcatheter approach.
Exclusion: Known prior vascular stenosis or dissection or injury to vessels intended to be catheterized during study procedures; Known contraindication to intravascular contrast material that cannot be adequately controlled with pre-medication; Subjects currently enrolled in another investigational device or drug study that clinically interferes with the current study endpoints; Known disorder of vascular fragility with propensity to vascular injury (e.g., Ehlers-Danlos syndrome); Acute phase myocardial infarction or uncontrolled cardiac arrhythmia; Bleeding disorder which limits the use of antiplatelet and/or anticoagulant therapy; Known hypersensitivity to Nickel; Uncontrolled serum electrolyte imbalance; Pregnancy or lactation.