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Terminated Phase 1Phase 2 Interventional

Prevention of Vascular Access Graft Failure in Patients With Chronic Renal Failure Requiring Hemodialysis

ClinicalTrials.gov ID: NCT00086164

Public ClinicalTrials.gov record NCT00086164. 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 Jul 21, 2026, 7:09 AM EDT

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

Official title

A Phase 1/2, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Pilot Trial to Assess the Effect of Treatment of the Recipient Vein of a Polytetrafluoroethylene (PTFE) Vascular Access Graft With Two Concentrations of E2F Decoy as Compared to Placebo on Neointimal Hyperplasia and the Preservation of Graft Function in Patients With Chronic Renal Failure Requiring Hemodialysis

Study identification

NCT ID
NCT00086164
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Anesiva, Inc.
Industry
Enrollment
Not listed

Conditions and interventions

Interventions

  • edifoligide (E2F Decoy) Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 79 Years
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
Apr 30, 2004
Primary completion
Not listed
Completion
Not listed
Last update posted
Jul 18, 2005

Started 2004

United States locations

U.S. sites
21
U.S. states
12
U.S. cities
18
Facility City State ZIP Site status
National Institute of Clinical Research, American Medical Tower Los Angeles California 90017
Outcomes Research International, Inc. Hudson Florida 34667
University of Miami, School of Medicine Miami Florida 33136
Tampa General Hospital Tampa Florida 33600
LifeLink Transplant Institute Tampa Florida 33606
Emory University, Renal Division Atlanta Georgia 30322
University Transplant Chicago Illinois 60612
Stoney Island Dialysis Chicago Illinois 60617
Methodist Hospital, Tower Surgical Indianapolis Indiana 46202
Vascular Surgery Associates Baton Rouge Louisiana 70808
Tulane Center for Abdominal Transplant New Orleans Louisiana 70112
Henry Ford Hospital Detroit Michigan 48202
Thoracic & Cardiovascular Healthcare Foundation Lansing Michigan 48910
St. Louis University, Division of Nephrology St Louis Missouri 63110
NYU Medical Center New York New York 10016
St. Luke's Hospital, Department of Surgery New York New York 10025
University of Rochester, The Center for Vascular Disease Rochester New York 14642
Montefiore Medical Center The Bronx New York 10467
Surgical Education Greenville South Carolina 29605
University of Utah School of Medicine, Dept of Surgery Salt Lake City Utah 84132
Nephrology Clinical Research Center Charlottesville Virginia 22908

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 NCT00086164, 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 Jul 18, 2005 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00086164 live on ClinicalTrials.gov.

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