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Biomime Stent in All-comers PCI Patients Registry (BELLINI)

U

University Hospital Maggiore della Carità of Novara

Status

Unknown

Conditions

Coronary Artery Disease

Treatments

Device: percutaneous coronary intervention

Study type

Observational

Funder types

Other

Identifiers

NCT02398955
BELLINI01

Details and patient eligibility

About

Biomime stent is a novel sirolimus-eluting stent (SES) (Meril Life Sciences Pvt. Ltd., Gujarat, India) with an ultra-thin stent platform (65 μm) and a biodegradable polymer licensed for the treatment of de novo coronary lesions. However no data regarding the efficacy and safety of this stent in an "all-comers" patient population treated with percutaneus coronary interventions (PCI) have been published so far. In this registry the investigators aimed to collect clinical and angiographic information about an extensive "all-comers" employ of this novel stent.

Enrollment

250 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • any coronary artery disease treated with percutaneous coronary intervention and a Biomime stent

Exclusion criteria

  • patients <18 years old

Trial design

250 participants in 1 patient group

Study cohort
Description:
All comers patients with coronary artery disease treated with percutaneous coronary intervention and at least one Biomime stent
Treatment:
Device: percutaneous coronary intervention

Trial contacts and locations

1

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Central trial contact

Alessandro Lupi, MD

Data sourced from clinicaltrials.gov

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