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FRED Study

Clinical Trial Title: 
FRED: Pivotal study of the MicroVention Flow Re-Direction Endoluminal Device stent system in the treatment of intracranial aneurysms
Clinical Trial Protocol ID: 
Clinical Trial Investigator Name: 
Demetrius Lopes, MD
Clinical Trial Protocol Description: 

To evaluate the safety and effectiveness of the MicroVention FRED system when used in the treatment of wide-necked intracranial aneurysms.

Clinical Trial Eligibility Criteria: 

In order to participate you must meet the following criteria:

  • Are 22 to 75 years.
  • Are a poor candidate for open surgical treatment because of prior surgical procedures or comorbidities limiting conventional surgical options.
  • Existing endovascular options (coiling, stent-assisted-coiling) would be ineffective because aneurysm is predisposed to recurrence.

This is a partial list of elgibility requirements. To inquire about your eligibility, please call the contact number provided. 

Clinical Trial Area: 
Stroke and Cerebrovascular Disease
Contact Phone: 
(312) 942-1114
Contact Name: 
Bartosz Jacher