Coronary Artery Disease Clinical Trial
Official title:
Retrospective, Observational Register to Investigate the Procedural and Post Procedural Implantation of Bioabsorbable Magnesium Scaffolds MAGMARIS (MAGIC Registry)
The retrospective study will investigate the clinical performance and long-term safety of scaffold implantation in a real world setting including high volume PCI centers in Italy
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 retrospective study is to investigate the clinical performance
and long-term safety of scaffold in a real world setting.
Institution involved in the present registry are high volume PCI centers. Operators have
experience in PCI with bioresorbable scaffolds technology
The study organization is based on:
DATA SAFETY MONITORING BOARD (DSMB) All adverse events will be reported to the DSMB and
reviewed on an on-going basis throughout the subject enrolment and follow-up period to ensure
the safety of subjects enrolled in this study. In case of clinical events, coronary artery
angiographies and percutaneous coronary interventions was reviewed by an independent
core-lab.
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