NCT00914979

AngioSculpt Scoring Balloon Catheter For Bifurcation Coronary Lesions (ABC Study)

AngioSculpt Scoring Balloon Catheter For Bifurcation Coronary Lesions (ABC Study) Prospective, Multi-center, Non-randomized, Single-arm Registry

• Status: Terminated
• Phase: Phase 3
• Study type: Interventional
• Enrollment: 7 (actual)
• Sponsor: HaEmek Medical Center, Israel · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

Assess the impact of lesion preparation using the AngioSculpt balloon in the treatment of bifurcation lesions in native coronary arteries.

Detailed description

The purpose of the AngioSculpt® Scoring Balloon Catheter For Bifurcation Coronary lesions (ABC registry) is to demonstrate the acute procedural success, device performance and long term outcome associated with use of the AngioSculpt Scoring Balloon Catheter (AngioScore, Inc., Fremont, CA) for lesion preparation in the treatment of bifurcation lesions in native coronary arteries

Conditions

• Bifurcation Coronary Disease

Interventions

Type	Name	Description
DEVICE	AngioSculpt	The AngioSculpt Scoring Balloon Catheter is a standard balloon dilatation catheter with a scoring balloon near the distal tip

Timeline

• Start date: 2008-09-01
• Primary completion: 2011-08-01
• Completion: 2011-09-01
• First posted: 2009-06-05
• Last updated: 2015-06-23

Locations

4 sites across 1 country: Israel