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AngioSculpt® Coronary Bifurcation Study

NCT00686647 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 93

Last updated 2011-08-10

Study results available
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Summary

The purpose of this study is to evaluate a new angioplasty catheter, AngioSculpt® for the treatment of bifurcation lesions (blockages occurring at branch points) in coronary arteries.

Conditions

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

Sponsors & Collaborators

  • AngioScore, Inc.

    lead INDUSTRY

Principal Investigators

  • Jeffrey W. Moses, M.D. · Columbia University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-04-30
Primary Completion
2010-04-30
Completion
2011-01-31

Countries

  • United States

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00686647 on ClinicalTrials.gov