Clinical Trials Directory

Trials / Completed

CompletedNCT01472705

Everolimus- Versus Biolimus-Eluting Stents in All-Comers

Long-Term Comparison of Everolimus-Eluting and Biolimus-Eluting Stents in All-Comer Patients

Status
Completed
Phase
Study type
Observational
Enrollment
814 (actual)
Sponsor
University of Freiburg · Academic / Other
Sex
All
Age
18 Years – 120 Years
Healthy volunteers
Not accepted

Summary

This study sought to investigate safety and efficacy of biolimus-eluting stents (BES) with biodegradable polymer as compared with everolimus-eluting stents (EES) with durable polymer through 3 years of follow-up.

Detailed description

A group of 814 consecutive patients undergoing percutaneous coronary intervention (PCI) was enrolled between 2007 and 2010, of which 527 were treated with EES and 287 with BES implantation. Clinical outcome was compared in 200 pairs using propensity score matching. The primary endpoint was a composite of death, myocardial infarction (MI) and target vessel revascularisation (TVR) at two-year follow-up.

Conditions

Timeline

Start date
2010-11-01
Primary completion
2010-11-01
Completion
2011-11-01
First posted
2011-11-16
Last updated
2015-12-03

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT01472705. Inclusion in this directory is not an endorsement.