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Neurovascular Self-Expanding Retrievable Stent System Study

Clinical Trial Title: 
Pivotal study of the Microvention Inc. neurovascular self-expanding retrievable stent system LVIS
Clinical Trial Protocol ID: 
Clinical Trial Investigator Name: 
Demetrius Lopes, MD
Clinical Trial Protocol Description: 

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.

Clinical Trial Eligibility Criteria: 

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.

Clinical Trial Area: 
Stroke and Cerebrovascular Disease
Contact Email: 
Contact Phone: 
(312) 942-1489
Contact Name: 
Christy Anton, CCRC