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Bare Metal Stent Versus Drug Coated Balloon With Provisional Stenting in Non-ST-Elevation Myocardial Infarction — PEPCADNSTEMI  

Coronary Heart Disease Clinical Trial

Official title:
Bare Metal Stent Versus Drug Coated Balloon With Provisional Stenting in Non-ST-Elevation Myocardial Infarction

Clinical Trial Summary

The aim of the present trial is to assess the efficacy of the standalone use of SeQuent(R) Please coated balloon compared to a bare metal stent (BMS) in patients with NSTEMI.

Clinical Trial Description

The aim of the present trial is to assess the efficacy of the standalone use of SeQuent(R) Please coated balloon compared to a bare metal stent (BMS) in patients with NSTEMI. Primary efficacy endpoint will be MACE (cardiac mortality, reinfarction, and target lesion revascularization) after 9 months. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01489449
Study type Interventional
Source Universität des Saarlandes
Contact
Status Completed
Phase Phase 4
Start date December 2012
Completion date June 23, 2022
View Details
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