CRE8 in All Comers Patients

NACompletedINTERVENTIONAL
Enrollment

215

Participants

Timeline

Start Date

October 31, 2012

Primary Completion Date

July 31, 2014

Study Completion Date

August 31, 2014

Conditions
Consecutive Subjects Who Are Suitable for a CoronaryAngioplasty of de Novo Lesion(s) in Native CoronaryArteries Should be Screened for Eligibility.A Total Number of 200 Patients Fulfilling the SelectionCriteria and Willing to Sign the Informed Consent Shouldbe Enrolled in the Trial.
Interventions
DEVICE

CR8 a drug eluting coronary stent

a drug eluting coronary device, made of Cobalt-Chromium alloy and integrally coated with i-Carbofilm™, loaded with formulated Sirolimus

Trial Locations (1)

64329

Tel Aviv Sourasky Medical Center, Tel Aviv

All Listed Sponsors
lead

Tel-Aviv Sourasky Medical Center

OTHER_GOV

NCT01687075 - CRE8 in All Comers Patients | Biotech Hunter | Biotech Hunter