Neurovascular Self-Expanding Retrievable Stent System Study
The purpose of this study is to evaluate the safety and efficacy of the Low Profile Visualized Intraluminal Support (LVIS and LVIS Jr.) devices from MicroVention Inc. when used to facilitate endovascular coiling of wide-necked intracranial aneurysms with coils.
In order to participate you must meet the following criteria:
- Are between 18 and 75 years.
- Have an unruptured or ruptured (>30days since occurence), wide-necked (neck ≥4mm or dome to neck ratio <2) intracranial saccular aneurysm (<20mm maximum diameter in any plane).
This is a partial list of elgibility requirements. To inquire about your eligibility, please call the contact number provided. If you wish to inquire via email, please include the title of the study in your message.