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Sprinter Legend Balloon Catheter

NCT00961311 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 51

Last updated 2011-10-26

Study results available
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Summary

Open label, single-arm trial to study the safety and effectiveness of the Sprinter Legend 1.25 mm angioplasty balloon.

Conditions

Interventions

PROCEDURE

Percutaneous Coronary Intervention

Balloon angioplasty of a severely stenotic coronary lesion with the Sprinter Legend 1.25mm Balloon.

DEVICE

Sprinter Legend 1.25mm Balloon Catheter

Balloon Angioplasty

Sponsors & Collaborators

  • Medtronic Vascular

    lead INDUSTRY

Principal Investigators

  • David Kandzari, MD · Scripps Green Hospital

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-08-31
Primary Completion
2010-01-31
Completion
2010-01-31

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 NCT00961311 on ClinicalTrials.gov