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BIOFLOW-SV Portugal Registry — BIOFLOW-SV  

Ischemic Heart Disease Clinical Trial

Official title:
BIOTRONIK - SaFety and Performance Registry for an Allcomers Patient Population With the SiroLimus Eluting Orsiro Stent Within Daily Clinical Practice in Small Vessels - Portugal Registry

Clinical Trial Summary

Assessment of the clinical safety and performance of the Orsiro drug-eluting stent in a real world setting in patients with small vessels with reference vessel diameter ≤2.75 mm

Clinical Trial Description

Prospective, single-arm, multi-center, all-comers registry with clinical follow-up visits at the hospital or by phone at 6 and 12 months post-procedure. A minimum of 1000 patients will be enrolled in approximately 15 sites in Brazil, including at least 415 patients with reference vessel diameter ≤2.75 mm as assessed by online QCA. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03600961
Study type Observational
Source Biotronik AG
Contact
Status Terminated
Phase
Start date July 5, 2018
Completion date December 21, 2021
View Details
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