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Completed Phase 4 Interventional

A Prospective, Multi-center, Single Arm Study Evaluating the Express™ Renal Premounted Stent System in the Treatment of Atherosclerotic Lesions in the Aortorenal Ostium.

ClinicalTrials.gov ID: NCT00597142

Public ClinicalTrials.gov record NCT00597142. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 10, 2026, 3:17 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to demonstrate superior 9-month binary restenosis rate of the Express™ Renal Premounted Stent System as compared to an Objective Performance Criterion representative of PTRA, for atherosclerotic lesions in the aortorenal ostium.

Study identification

NCT ID
NCT00597142
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Boston Scientific Corporation
Industry
Enrollment
100 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 2004 (Type not available)
Primary completion
Jul 2005 (Actual)
Completion
Oct 2009 (Actual)
Last update posted
Nov 21, 2014

2004 – 2009

United States locations

U.S. sites
14
U.S. states
11
U.S. cities
13
Facility City State ZIP Site status
Sarasota Memorial Hospital Care System Sarasota Florida 34239 —
Peoria Radiology Associates Research & Education Foundation Peoria Illinois 61637 —
Prairie Education & Research Cooperative Springfield Illinois 62701 —
St. Vincent Hospital & Health Care Center, Inc. Indianapolis Indiana 46260 —
The Care Group, LLC Indianapolis Indiana 46260 —
Cardiovascular Institute of the South (CIS) Lafayette Louisiana 70506 —
Ochsner Clinic Foundation New Orleans Louisiana 70121 —
NYPH & Trustees of Columbia University of New York New York New York 10032 —
WakeMed Raleigh North Carolina 27610 —
Philadelphia Health and Education Corp. d/b/a Drexel University College of Medicine Philadelphia Pennsylvania 19102 —
Greenville Hospital System Greenville South Carolina 29605 —
North Central Heart Institute Sioux Falls South Dakota 57108 —
St. Luke's Episcopal Hospital Houston Texas 77030 —
CAMC Institute Charleston West Virginia 25304 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00597142, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 21, 2014 · Synced Nov 10, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00597142 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →