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BIOTRONIKS - Safety and Performance in de NOvo Lesion of NatiVE Coronary Arteries With Magmaris- Registry: BIOSOLVE-IV — BIOSOLVE-IV  

Coronary Artery Disease Clinical Trial

Official title:
BIOTRONIKS - Safety and Performance in de NOvo Lesion of NatiVE Coronary Arteries With Magmaris- Registry: BIOSOLVE-IV

Clinical Trial Summary

The registry will investigate the clinical performance and long-term safety of Magmaris in a real world setting

Clinical Trial Description

Coronary stents are the default devices for the treatment of coronary artery disease in percutaneous coronary intervention (PCI) according to existing guidelines. However, thrombosis and restenosis are still the main limitations of current permanent metallic stents. In contrast to Bare Metal Stents (BMSs), Drug Eluting Stents (DESs) have a reduced restenosis rate due to the presence of antiproliferative agents in the coating layer of the stent surface and reduced rate of repeat revascularisation. However, late and very late stent thrombosis remains the limitation of DES in spite of prolonged dual antiplatelet therapy.Bioabsorbable scaffolds have been introduced to overcome limitations of permanent metallic stents. The aim of this observational registry is to investigate the clinical performance and long-term safety of Magmaris in a real world setting. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02817802
Study type Observational [Patient Registry]
Source Biotronik AG
Contact
Status Active, not recruiting
Phase
Start date August 2016
Completion date October 2025
View Details
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