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Completed Not applicable Interventional

GORE-TEX PROPATEN Vascular Graft Study

ClinicalTrials.gov ID: NCT00205790

Public ClinicalTrials.gov record NCT00205790. 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 6, 2026, 3:00 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

Comparison of Primary Patency Between GORE-TEX PROPATEN Vascular Grafts and Thin Walled GORE-TEX Stretch Vascular Grafts

Brief summary

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

To demonstrate equivalence in patency performance of GORE-TEX PROPATEN Vascular Grafts and Thin Walled GORE-TEX Stretch Vascular Grafts in a peripheral bypass application to support a claim of substantial equivalence.

Study identification

NCT ID
NCT00205790
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
W.L.Gore & Associates
Industry
Enrollment
200 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
21 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 31, 2003
Primary completion
Not listed
Completion
Jul 31, 2007
Last update posted
Aug 6, 2008

2003 – 2007

United States locations

U.S. sites
18
U.S. states
14
U.S. cities
17
Facility City State ZIP Site status
Georgetown University Hospital Washington D.C. District of Columbia 20007
Memorial Regional Hospital Hollywood Florida 33028
St. Vincent's Hospital Jacksonville Florida 32204
Sacred Heart Hospital Pensacola Florida 32504
Medical Center of Central Georgia Macon Georgia 31201
Jewish Hospital Louisville Kentucky 40202
Upper Chesapeake Medical Center Baltimore Maryland 21014
Baystate Medical Center Springfield Massachusetts 01107
Mercy Medical Center Springfield Massachusetts 01107
William Beaumont Hospital Bingham Farms Michigan 48025
Borgess Hospital Kalamazoo Michigan 49048
University of Mississippi Medical Center Jackson Mississippi 39216
Morristown Memorial Hospital Morristown New Jersey 07960
Maimonides Hospital Brooklyn New York 11219
Ohio State University Medical Center Columbus Ohio 43210
Wilkes-Barre General Hospital Plains Pennsylvania 18705
Baptist East Hospital Memphis Tennessee 38120
Charleston Area Medical Center 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 NCT00205790, 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 6, 2008 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00205790 live on ClinicalTrials.gov.

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