NCT04323033 - Safety and Efficacy of Peripheral, Cobalt-chromium Sirolimus Eluting Stent (PERS) Versus Cobalt-chromium Stent (Neptune C) | Biotech Hunter

Enrollment

Participants

Timeline

Start Date

March 13, 2019

Primary Completion Date

October 31, 2020

Study Completion Date

November 9, 2021

Conditions

Peripheral Arterial Disease

Interventions

DEVICE

PERS stent

"PERS® is a cobalt-chromium stent, made of cobalt-chromium alloy with drug (Sirolimus) and biodegradable polymer controlling drug elution.~The length of the stent is selected to cover the treated lesion with a margin of 5 mm proximal and distal, while the diameter of the stent will be selected based on the QVA measurement (balloon to vessel ratio 1:1)."

DEVICE

NEPTUN C stent

Neptun C is balloon-expanding cobalt-chromium stent.

Trial Locations (3)

32-500

Małopolskie Centrum Sercowo-Naczyniowe PAKS American Heart of Poland S.A., Chrzanów

20-081

Samodzielny Publiczny Szpital Kliniczny nr 1, Lublin

86-031

Szpital Eskulap Centrum Leczenia Chorób Serca i Naczyń, Osielsko