Solitaire Aneurysm Remodeling Registry

Medtronic Neurovascular Clinical Affairs

Overview

The objective of the registry is to evaluate the effectiveness and performance of the Solitaire Neurovascular Remodeling Device when used with embolic coils in the treatment of intracranial aneurysms.

Study Type

OBSERVATIONAL

Conditions

Intracranial Saccular Aneurysm, Either Rupture or Unruptured Wide Neck Aneurysm

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Confirmed diagnosis of intracranial saccular aneurysms, either ruptured or unruptured * Aneurysm requires current treatment with coils and a stent or aneurysm hs been previously treated with coils, but no prior placement of a stent. * Aneurysm has a wide neck defined as having a neck equal to or greater than 4mm or a dome-to-neck ratio of \<2. * Patient is 18 years or older. * Patient has a Hunt \& Hess score of III or less. Exclusion Criteria: * Patient has a fusiform or dissecting aneurysm type. * Patient is contraindicated for either heparin or anti-platelet therapy. * Patient has severe allergy to IV contrast medium. * Patient has a known hypersensitivity to nickel-titanium.

Locations (1)

Hopital Neurologique

Lyon, France

Outcomes

Primary Outcomes

Stable Stent placement with complete coverage across the aneurysm neck with parent artery patency

Time frame: Six months post-implant

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.