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ClinicalTrials.gov record
Not listed Phase 3 Interventional

A Multi-Centered, Two-Arm, Randomized Study Comparing the Effects of AAT-023 (Zuragen) Solution, and Heparin on the Incidence of Catheter Related Blood Stream Infections in Tunneled Chronic Central Venous Catheters for Dialysis

ClinicalTrials.gov ID: NCT00628680

Public ClinicalTrials.gov record NCT00628680. 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 Sep 3, 2026, 2:54 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

Pivotal/Phase III Multicentered, Two-Arm, Randomized Study Comparing the Effects of AAT-023 Solution (Zuragen), and Heparin on the Incidence of Catheter Related Blood Stream Infections in Tunneled Chronic Central Venous Catheters for Dialysis

Brief summary

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

The purpose of this study is to determine if AAT-023 (Zuragen) solution is superior to Heparin in preventing Catheter Related Blood Stream Infections for End Stage Renal Disease patients.

Study identification

NCT ID
NCT00628680
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ash Access Technology
Industry
Enrollment
415 participants

Conditions and interventions

Interventions

Device · Drug

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
Jun 30, 2006
Primary completion
Jun 30, 2008
Completion
Not listed
Last update posted
Mar 4, 2008

Started 2006

United States locations

U.S. sites
22
U.S. states
11
U.S. cities
20
Facility City State ZIP Site status
Bakersfield Dialysis Center Bakersfield California 93309
Renal Medical Associates Lynwood California 90262
Nephrology & Hypertension Associates, PC Middlebury Connecticut 06762
Brandon nephrology Brandon Florida 33511
Gulf Breeze Dialysis Center Dunedin Florida 34698
Bayonet Point Hudson Kidney Center Hudson Florida 34667
Outcomes Research International, Inc. Hudson Florida 34667
Bay Breeze Dialysis Largo Florida 33778
New Port Richey Kidney Center New Port Richey Florida 34668
Discovery Medical Research Group Ocala Florida 34471
Nephrology consultants Orlando Florida 32806
Hernando Kidney Center Spring Hill Florida 34608
Nephrology Associates, P.C. Augusta Georgia 30901
MId Atlantic Nephrology Associates, PA Baltimore Maryland 21208
Caritas St. Elizabeth Center Boston Massachusetts 02135
Western New England Renal & Transplant Associatea Springfield Massachusetts 01107
Henry Ford Hospital Detroit Michigan 48202
Hypertension & Renal Research Group Buffalo New York 14225
Bayview Nephrology, Inc. Erie Pennsylvania 16507
Kidney Associates, PLLC Houston Texas 77030
Southwest Houston Research, LTD Houston Texas 77099
Fox Valley Nephrology Associates Appelton Wisconsin 54911

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 NCT00628680, 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 Mar 4, 2008 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00628680 live on ClinicalTrials.gov.

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