Recruitment

Recruitment Status
Active, not recruiting

Summary

Conditions
  • Acute Coronary Syndrome
  • High Bleeding Risk
Type
Interventional
Phase
Not Applicable
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Younger than 125 years
Gender
Both males and females

Description

In this study all patients will receive the BioFreedom™ Drug Coated Stent and one month of Dual Anti Platelet Therapy

In this study all patients will receive the BioFreedom™ Drug Coated Stent and one month of Dual Anti Platelet Therapy

Tracking Information

NCT #
NCT02843633
Collaborators
Not Provided
Investigators
Study Chair: Martin Leon Cardiovascular Research Foundation, New York Principal Investigator: Mitchell Krucoff Duke University Principal Investigator: Philip Urban Hôpital de la Tour