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Completed Phase 3 Interventional Results available

GORE VIABAHN Endoprosthesis Versus Percutaneous Transluminal Angioplasty (PTA) to Revise AV Grafts in Hemodialysis

ClinicalTrials.gov ID: NCT00737672

Public ClinicalTrials.gov record NCT00737672. 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 Oct 25, 2026, 12:33 PM EDT

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

Official title

GORE VIABAHN® Endoprosthesis Versus Percutaneous Transluminal Angioplasty (PTA) to Revise Arteriovenous Grafts at the Venous Anastomosis in Hemodialysis Patients

Brief summary

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

The objective of the study is to establish efficacy and safety of the GORE VIABAHN® Endoprosthesis with PROPATEN Bioactive Surface when used to revise arteriovenous (AV) prosthetic grafts at the venous anastomosis in the maintenance or re-establishment of vascular access for hemodialysis.

Study identification

NCT ID
NCT00737672
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
W.L.Gore & Associates
Industry
Enrollment
293 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
Sep 2008 (Type not available)
Primary completion
May 2011 (Actual)
Completion
Jun 2013 (Actual)
Last update posted
Oct 21, 2014

2008 – 2013

United States locations

U.S. sites
31
U.S. states
18
U.S. cities
29
Facility City State ZIP Site status
Not listed Birmingham Alabama 35249 —
Not listed Fresno California 93710 —
Not listed Inglewood California 90301 —
Not listed Oceanside California 92056 —
Not listed Riverside California 92501 —
Not listed San Diego California 92115 —
Not listed San Diego California 92120 —
Not listed San Francisco California 94143 —
Not listed New Haven Connecticut 06520 —
Not listed Jacksonville Florida 32209 —
Not listed Albany Georgia 31707-1908 —
Not listed Chicago Illinois 60612-3833 —
Not listed Des Moines Iowa 50309 —
Not listed Louisville Kentucky 40202 —
Not listed Baltimore Maryland 21239 —
Not listed New Brighton Minnesota 55112 —
Not listed Saint Paul Minnesota 55101 —
Not listed Cincinnati Ohio 45212 —
Not listed Cincinnati Ohio 45267-0585 —
Not listed Dayton Ohio 45406 —
Not listed Portland Oregon 97210 —
Not listed Philadelphia Pennsylvania 19104 —
Not listed Charleston South Carolina 29421 —
Not listed Greenville South Carolina 29615 —
Not listed Beaumont Texas 77701 —
Not listed Houston Texas 77030 —
Not listed Norfolk Virginia 23507 —
Not listed Winchester Virginia 22601 —
Not listed Bellevue Washington 98004 —
Not listed Spokane Washington 99204 —
Not listed Milwaukee Wisconsin 53226 —

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 NCT00737672, 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 Oct 21, 2014 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00737672 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →