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The Study of the Crushing Technique Application Using SES in Coronary Bifurcations.

NCT00749424 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 350

Last updated 2010-02-04

No results posted yet for this study

Summary

The objective of this study is to compare the safety and effectiveness of two different approaches to treat bifurcational lesions with CYPHER SELECT™ Sirolimus-eluting Balloon-expandable Coronary Stent , Cordis Corp): a) the "crushing" technique to stent both branches vs. b) a provisional T stenting technique of the side branch.

Conditions

Interventions

DEVICE

SES

CYPHER SELECT™ Sirolimus-eluting Balloon-expandable Coronary Stent

DEVICE

SES

CYPHER SELECT™ Sirolimus-eluting Balloon-expandable Coronary Stent

Sponsors & Collaborators

  • Cordis Corporation

    lead INDUSTRY

Principal Investigators

  • Antonio Colombo, MD, PhD · Fondazione Centro San Raffaele del Monte Tabor

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-01-31
Primary Completion
2005-05-31
Completion
2009-04-30

Countries

  • Italy

Study Locations

More Related Trials

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 NCT00749424 on ClinicalTrials.gov