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Treatment Study of Intracranial Dural Arteriovenous Fistulas

Clinical Trial Title: 
PHIL dAVF: Study of Phill® Embolic System in the treatment of intracranial dural arteriovenous fistulas.
Clinical Trial Protocol ID: 
17111006
Clinical Trial Investigator Name: 
Michael Chen, MD
Clinical Trial Protocol Description: 

This study is a prospective, multicenter, single-arm study. Patients with dural arteriovenous fistulas (dAVF) have a few choices for safe treatment. In this study, all patients with qualifying dAVFs will be treated with PHIL® Liquid Embolic material.

Clinical Trial Eligibility Criteria: 

In order to participate you must meet the following criteria:

  • Are between 22 and 80 years of age.
  • Are willing and capable of complying with all study protocol requirements, including specified follow-up period.
  • Provide written informed consent (subject or authorized legal representative) prior to initiation of any study procedures.
  • Have an intracranial dAVF.

You will be excluded from the study if any of the following criteria apply to you:

  • Have multiple dAVFs to be treated.
  • Have a history of life threatening allergy to contrast media (unless treatment for allergy is tolerated).
  • Have known allergies to dimethylsulfoxide, iodine.
  • Are currently participating in another clinical study

This is a partial list of inclusion and exclusion criteria.

Clinical Trial Area: 
Stroke and Cerebrovascular Disease
Contact Phone: 
(312) 942-8681
Contact Name: 
Kevin Keegan