ClinicalTrials.gov record
Terminated Phase 4 Interventional

Plaque Removal Versus Open Bypass Surgery For Critical Limb Ischemia

ClinicalTrials.gov ID: NCT00504088

Public ClinicalTrials.gov record NCT00504088. 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 May 13, 2026, 6:41 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Study identification

NCT ID
NCT00504088
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
FoxHollow Technologies
Industry
Enrollment
Not listed

Conditions and interventions

Interventions

  • Bypass Procedure
  • Silverhawk Plaque Excision Procedure

Procedure

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
Sep 30, 2006
Primary completion
Not listed
Completion
Not listed
Last update posted
Aug 19, 2008

Started 2006

United States locations

U.S. sites
31
U.S. states
22
U.S. cities
29
Facility City State ZIP Site status
University of Alabama, Birmingham Birmingham Alabama 35294
Los Angeles Cardiology/Good Samaritan Los Angeles California 90017
UC Davis Vascular Center Sacramento California 95817
San Francisco VA Medical Center San Francisco California 94121
Stanford University Medical Center/Palo Alto VA Stanford California 94306
Heart & Vascular Clinic of Northern Colorado Fort Collins Colorado 80523
Holmes Regional Medical Center Melbourne Florida 32901
Sacred Heart Hospital Pensacola Florida 32504
University of Chicago Chicago Illinois 60637
Advocate Christ Medical Center Oak Lawn Illinois 60453
St. Vincent Indianapolis Indiana 46260
Iowa Methodist Medical Center Des Moines Iowa 50309
Vascular Surgery Associates Baton Rouge Louisiana 70809
Beth Isreal (BIDMC) Boston Massachusetts 02215
St. Vincent Hospital Worchester Massachusetts 01608
William Beaumont/Southeast Surgical Royal Oak Michigan 48073
Providence Hospital Southfield Michigan 48075
University of Mississippi Jackson Mississippi 39216
Alegent Health Research Center Omaha Nebraska 68152
Hackensack University Medical Center Hackensack New Jersey 07601
New Mexico Heart Institute, PA Albuquerque New Mexico 87102
St. Vincent's Medical Center New York New York 10011
NY Weill Cornell Medical Center New York New York 10021
Columbia Presbyterian New York New York 10604
Duke University Medical Center Durham North Carolina 27712
Cleveland VAMC Cleveland Ohio 44106
Thomas Jefferson University Hospital Philadelphia Pennsylvania 19107
Rhode Island Hospital Providence Rhode Island 02903
Vanderbilt University Medical Center Nashville Tennessee 37232
Sentara Heart Hospital Norfolk Virginia 23507
Madigan Army Medical Center Tacoma Washington 98431

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 NCT00504088, 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 Aug 19, 2008 · Synced May 13, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00504088 live on ClinicalTrials.gov.

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