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Advanta VXT and Flixene PMCF Registry

Recruiting · NCT07161583

Conditions: Peripheral Arterial Disease

At a glance

Research payments reported, 2025
$15,000
U.S. investigators named
1
Sites paid
1
Planned or actual enrollment
1,000

About the trial

Sponsor
Atrium Medical Corporation
Tested
Advanta VXT Vascular Graft (device), Flixene Vascular Graft (device)
Dates
Started 2025-09-25; completion 2027-12
Results posted
Not yet

The purpose of the registry is to evaluate the long-term safety and performance of Advanta VXT and Flixene vascular grafts for repair or replacement of peripheral arteries. This registry is also intended to provide further data on the clinical usefulness of the Advanta VXT and Flixene vascular grafts.

From ClinicalTrials.gov, last updated 2026-09-11. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Atrium Medical Corporation reported $15,000 in research payments for this study in 2025 (1 payments).

Products named: Flixene

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.