AngioSculpt® Coronary Bifurcation Study

NACompletedINTERVENTIONAL
Enrollment

93

Participants

Timeline

Start Date

April 30, 2008

Primary Completion Date

April 30, 2010

Study Completion Date

January 31, 2011

Conditions
Coronary Artery DiseaseMyocardial Ischemia
Interventions
DEVICE

AngioSculpt® Scoring Balloon Catheter

Use of a stent for the main branch of a bifurcation lesion and use of a scoring balloon for the side branch of the same bifurcation lesion

DEVICE

AngioSculpt Scoring Balloon Catheter

Treatment of the side-branch vessel of true bifurcation lesions using the AngioSculpt device

Trial Locations (1)

10032

Columbia University Medical Center, New York

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AngioScore, Inc.

INDUSTRY

NCT00686647 - AngioSculpt® Coronary Bifurcation Study | Biotech Hunter | Biotech Hunter