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BIOTRONIK Dynetic-35 Stent for the Treatment of Peripheral Iliac Lesions — BIONETIC-I  

Peripheral Artery Disease Clinical Trial

Official title:
BIOTRONIK Dynetic-35 for the Treatment of Peripheral Iliac Lesions, Using the Cobalt Chromium Balloon-expandable Dynetic-35 Stent in Association With Passeo-35 Xeo Peripheral Dilation Catheter

Clinical Trial Summary

BIOTRONIK cobalt chromium balloon-expandable Dynetic-35 stent in association with Passeo-35 Xeo peripheral dilation catheter for the treatment of peripheral iliac lesions

Clinical Trial Description

Prospective, international, multi-center, single-arm study with up to 60 months follow up to evaluate safety and effectiveness of BIOTRONIK's Dynetic-35 stent associated with the use of Passeo-35 Xeo for the treatment of peripheral artery disease (PAD) in subjects with atherosclerotic disease in iliac arteries ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04830228
Study type Observational
Source Biotronik AG
Contact
Status Active, not recruiting
Phase
Start date August 10, 2021
Completion date February 28, 2028
View Details
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