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A Feasibility Study of the Cordis Neurovascular Self Expanding Stent System in Intracranial Arteries

NCT00349908 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2014-06-30

Study results available
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Summary

Feasibility study to assess safety of treating patients with self expanding stent in intracranial arteries.

Conditions

Interventions

DEVICE

Cordis Neurovascular ENTERPRISE Self Expanding Stent System

Implantation of the device ENTERPRISE used to treat symptomatic stenosis in intracranial arteries.

DEVICE

Cordis Neurovascular ENTERPRISE Self Expanding Stent System

Implantation of the device ENTERPRISE to treat wide-necked aneurysms

Sponsors & Collaborators

  • Codman & Shurtleff

    lead INDUSTRY

Principal Investigators

  • Pedro Lylyk, MD · ENERI-CLINICA ADVENTISTA BELGRANO

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-09-30
Primary Completion
2008-10-31
Completion
2009-03-31

Countries

  • Argentina

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 NCT00349908 on ClinicalTrials.gov