PHIL Evaluation in the Endovascular Treatment of Intracranial Dural AVF

  • days left to enroll
  • participants needed
  • sponsor
    Microvention-Terumo, Inc.
Updated on 8 December 2019
Primary Contact
CHU Limoges (1.2 mi away) Contact
+14 other location


The primary objective of this study is to demonstrate the safety and efficacy of the PHIL liquid in endovascular treatment of dural arteriovenous fistula.


This is an European multi-center observational study. Treatments and follow-up visits will be done as per standard of care.

The objective of this study is to evaluate the efficacy and safety of the PHIL device in the treatment of intracranial dural ArterioVenous Fistula (dAVF). The PHIL device, a non-adhesive liquid embolic agent, has been CE marked since July 2014. It is intended for use in the embolization of lesions in the peripheral and neurovasculature, including arteriovenous malformations and hypervascular tumors.

All patients with an intracranial dAVF that has not been previously treated and will be treated by embolization with PHIL are eligible for this study. A maximum of 70 patients will be enrolled in this study in 16 European Institutions.

The expected approximate study duration is 38 months.

Clinical Study IdentifierNCT03317821
SponsorMicrovention-Terumo, Inc.
Last Modified on8 December 2019

Adding a note
adding personal notes guide

Select a piece of text and start making personal notes.


Yes No Not Sure

Inclusion Criteria

Is your age greater than or equal to 18 yrs?
Gender: Male or Female
Do you have Persistent cerebral embryonic artery?
Patient or patient's legally authorized representative has received information about data collection and has signed and dated an Informed Consent Form
Patient has an intracranial dAVF that can be treated by embolization with PHIL used with or without other embolization products except other non-adhesive liquid embolic agents (i.e. Squid, Onyx)
Patient is at least 18 years of age

Exclusion Criteria

Patient has multiple dAVFs to be treated
Patient participates in a study evaluating another medical device, procedure, or medication during the course of dAVF treatment and follow-up per the study protocol
Patient does not give consent to the collection and processing of data required for centralized monitoring
Any condition that could prevent patient follow up
Clear my responses

How to participate?

Step 1 Connect with a site
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact


Phone Email

Please verify that you are not a bot.
Step 2 Get screened

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more
Step 3 Enroll in the clinical study

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more
Step 4 Get your study results

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider


Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer


user name

Annotated by • 



Reply by • Private

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.

No made yet