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PHIL in the Treatment of Intracranial dAVF.

Completed · Not applicable · NCT03467542

Conditions: Arteriovenous Dural Fistula

At a glance

Research payments reported, 2025
$18,760
U.S. investigators named
6
Sites paid
6
Planned or actual enrollment
64

About the trial

Sponsor
Microvention-Terumo, Inc.
Tested
PHIL® Liquid Embolic System (device)
Dates
Started 2018-08-24; completion 2022-12-12
Results posted
Yes

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

From ClinicalTrials.gov, last updated 2024-12-31. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Microvention, Inc. reported $18,760 in research payments for this study in 2025 (7 payments).

Products named: Stent, Phil

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.