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Carotid Artery Stenting With Protection Registry

NCT00318851 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 62

Last updated 2010-08-26

No results posted yet for this study

Summary

The purpose of this study is to evaluate ischemic events and neuropsychological changes after carotid artery angioplasty and stenting with a neuroprotection device.

Conditions

  • Carotid Artery Stenosis

Interventions

DEVICE

Carotid Stent with Distal Protection Device

Carotid Stent Placement with Distal Protection

Sponsors & Collaborators

  • Providence Health & Services

    lead OTHER

Principal Investigators

  • Rodney D. Raabe, MD · Providence Health & Services

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2003-09-30
Primary Completion
2007-08-31
Completion
2007-08-31

Countries

  • United States

Study Locations

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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 NCT00318851 on ClinicalTrials.gov