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GORE-TEX PROPATEN Vascular Graft Study

Primary Purpose

Peripheral Vascular Diseases

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Vascular graft
Sponsored by
W.L.Gore & Associates
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peripheral Vascular Diseases

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patient requires primary above-knee bypass where the proximal anastomosis will be to the common femoral or proximal superficial femoral artery and the distal anastomosis will be the popliteal artery proximal to the medial head of the gastrocnemius; Patient has Grade III or IV occlusive vascular disease; Patient has a postoperative life expectancy greater than one year; Patient is at least 21 years of age; Patient is able to comply with all study requirements and be available for follow-up visits at 1 month, 6 months and 12 months post procedure; Patient is willing and able to provide written, informed consent. Exclusion Criteria: Patient had a previous bypass in the diseased extremity (below iliacs); Patient has known coagulation disorders including hypercoagulability; Patient has had any previous instance of Heparin Induced Thrombocytopenia type 2 (HIT-2) or has known hypersensitivity to heparin; Patient has an acute embolic arterial occlusion; Patient requires sequential extremity revascularizations or other procedures that require use of additional vascular grafts; Patient had percutaneous transluminal angioplasty to the implant site within the previous 30 days; Patient is in need of, or is scheduled for, a cardiac surgical procedure or a different vascular surgical procedure; Patient has active infection in the region of graft placement; or Patient has an incomplete preoperative assessment (as outlined in this protocol) due to an emergency procedure, a traumatic injury or any other reason.

Sites / Locations

  • Georgetown University Hospital
  • Memorial Regional Hospital
  • St. Vincent's Hospital
  • Sacred Heart Hospital
  • Medical Center of Central Georgia
  • Jewish Hospital
  • Upper Chesapeake Medical Center
  • Baystate Medical Center
  • Mercy Medical Center
  • William Beaumont Hospital
  • Borgess Hospital
  • University of Mississippi Medical Center
  • Morristown Memorial Hospital
  • Maimonides Hospital
  • Ohio State University Medical Center
  • Wilkes-Barre General Hospital
  • Baptist East Hospital
  • Charleston Area Medical Center

Outcomes

Primary Outcome Measures

Primary patency at 12 months
Major device complication rates at 12 months

Secondary Outcome Measures

Technical failures
Secondary patency

Full Information

First Posted
September 12, 2005
Last Updated
August 6, 2008
Sponsor
W.L.Gore & Associates
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1. Study Identification

Unique Protocol Identification Number
NCT00205790
Brief Title
GORE-TEX PROPATEN Vascular Graft Study
Official Title
Comparison of Primary Patency Between GORE-TEX PROPATEN Vascular Grafts and Thin Walled GORE-TEX Stretch Vascular Grafts
Study Type
Interventional

2. Study Status

Record Verification Date
August 2008
Overall Recruitment Status
Completed
Study Start Date
February 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
W.L.Gore & Associates

4. Oversight

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Vascular Diseases

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Single
Allocation
Randomized
Enrollment
200 (false)

8. Arms, Groups, and Interventions

Intervention Type
Device
Intervention Name(s)
Vascular graft
Primary Outcome Measure Information:
Title
Primary patency at 12 months
Title
Major device complication rates at 12 months
Secondary Outcome Measure Information:
Title
Technical failures
Title
Secondary patency

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient requires primary above-knee bypass where the proximal anastomosis will be to the common femoral or proximal superficial femoral artery and the distal anastomosis will be the popliteal artery proximal to the medial head of the gastrocnemius; Patient has Grade III or IV occlusive vascular disease; Patient has a postoperative life expectancy greater than one year; Patient is at least 21 years of age; Patient is able to comply with all study requirements and be available for follow-up visits at 1 month, 6 months and 12 months post procedure; Patient is willing and able to provide written, informed consent. Exclusion Criteria: Patient had a previous bypass in the diseased extremity (below iliacs); Patient has known coagulation disorders including hypercoagulability; Patient has had any previous instance of Heparin Induced Thrombocytopenia type 2 (HIT-2) or has known hypersensitivity to heparin; Patient has an acute embolic arterial occlusion; Patient requires sequential extremity revascularizations or other procedures that require use of additional vascular grafts; Patient had percutaneous transluminal angioplasty to the implant site within the previous 30 days; Patient is in need of, or is scheduled for, a cardiac surgical procedure or a different vascular surgical procedure; Patient has active infection in the region of graft placement; or Patient has an incomplete preoperative assessment (as outlined in this protocol) due to an emergency procedure, a traumatic injury or any other reason.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Enrico Ascher, MD
Organizational Affiliation
Maimonides Hospital, Brooklyn NY
Official's Role
Principal Investigator
Facility Information:
Facility Name
Georgetown University Hospital
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20007
Country
United States
Facility Name
Memorial Regional Hospital
City
Hollywood
State/Province
Florida
ZIP/Postal Code
33028
Country
United States
Facility Name
St. Vincent's Hospital
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32204
Country
United States
Facility Name
Sacred Heart Hospital
City
Pensacola
State/Province
Florida
ZIP/Postal Code
32504
Country
United States
Facility Name
Medical Center of Central Georgia
City
Macon
State/Province
Georgia
ZIP/Postal Code
31201
Country
United States
Facility Name
Jewish Hospital
City
Louisville
State/Province
Kentucky
ZIP/Postal Code
40202
Country
United States
Facility Name
Upper Chesapeake Medical Center
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21014
Country
United States
Facility Name
Baystate Medical Center
City
Springfield
State/Province
Massachusetts
ZIP/Postal Code
01107
Country
United States
Facility Name
Mercy Medical Center
City
Springfield
State/Province
Massachusetts
ZIP/Postal Code
01107
Country
United States
Facility Name
William Beaumont Hospital
City
Bingham Farms
State/Province
Michigan
ZIP/Postal Code
48025
Country
United States
Facility Name
Borgess Hospital
City
Kalamazoo
State/Province
Michigan
ZIP/Postal Code
49048
Country
United States
Facility Name
University of Mississippi Medical Center
City
Jackson
State/Province
Mississippi
ZIP/Postal Code
39216
Country
United States
Facility Name
Morristown Memorial Hospital
City
Morristown
State/Province
New Jersey
ZIP/Postal Code
07960
Country
United States
Facility Name
Maimonides Hospital
City
Brooklyn
State/Province
New York
ZIP/Postal Code
11219
Country
United States
Facility Name
Ohio State University Medical Center
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
Facility Name
Wilkes-Barre General Hospital
City
Plains
State/Province
Pennsylvania
ZIP/Postal Code
18705
Country
United States
Facility Name
Baptist East Hospital
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38120
Country
United States
Facility Name
Charleston Area Medical Center
City
Charleston
State/Province
West Virginia
ZIP/Postal Code
25304
Country
United States

12. IPD Sharing Statement

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GORE-TEX PROPATEN Vascular Graft Study

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