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Plaque Removal Versus Open Bypass Surgery For Critical Limb Ischemia (PROOF)

Primary Purpose

Peripheral Vascular Diseases

Status
Terminated
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Bypass
Silverhawk Plaque Excision
Sponsored by
FoxHollow Technologies
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peripheral Vascular Diseases focused on measuring CLI, Critical Limb Ischemia, PAD, Peripheral Arterial Disease, Artherosclerosis, Leg Pain, Cardiovascular, Artherectomy, Bypass, Peripheral Bypass, PROOF

Eligibility Criteria

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

Inclusion Criteria:

  • Ischemic rest pain for more than 2 weeks or ulceration or gangrene of the foot or toes (Rutherford Becker Category 4, 5 or 6)
  • Willing and able, as evaluated by the PI, to provide Informed Consent
  • Willing to undergo up to 5 years of clinical follow up visits as scheduled
  • Angiographic pattern of infrainguinal disease that can be reasonably managed either by surgery or plaque excision in the first instance
  • Reconstitution of at least one patent target tibial segment below the knee which provides run-off to the foot
  • The patient must be >18 years of age
  • Target lesion(s) is located at or below the level of the superficial femoral artery
  • Target lesion(s) is >50% stenosed by quantitative vascular angiography
  • Ability to take at least one of the following types of medications: anti- platelet or anti-thrombotic therapy

Exclusion Criteria:

  • Patient has cardiac or cardiovascular comorbidities that would make surgery inappropriate
  • Patient has terminal or Stage 4 cancer
  • Patient has extensive gangrene that requires both a Below-the-Knee amputation and a revascularization procedure
  • Previous stent in the target lesion
  • Active infection at planned incision site
  • The patient is a pregnant woman
  • The patient has significant suprainguinal or Common Femoral disease that can not be treated either prior to or during the index procedure
  • Target Lesion is a Chronic Total Occlusion (CTO) that is greater than 15cm in length and has severe, continuous calcification

Sites / Locations

  • University of Alabama, Birmingham
  • Los Angeles Cardiology/Good Samaritan
  • UC Davis Vascular Center
  • San Francisco VA Medical Center
  • Stanford University Medical Center/Palo Alto VA
  • Heart & Vascular Clinic of Northern Colorado
  • Holmes Regional Medical Center
  • Sacred Heart Hospital
  • University of Chicago
  • Advocate Christ Medical Center
  • St. Vincent
  • Iowa Methodist Medical Center
  • Vascular Surgery Associates
  • Beth Isreal (BIDMC)
  • St. Vincent Hospital
  • William Beaumont/Southeast Surgical
  • Providence Hospital
  • University of Mississippi
  • Alegent Health Research Center
  • Hackensack University Medical Center
  • New Mexico Heart Institute, PA
  • St. Vincent's Medical Center
  • NY Weill Cornell Medical Center
  • Columbia Presbyterian
  • Duke University Medical Center
  • Cleveland VAMC
  • Thomas Jefferson University Hospital
  • Rhode Island Hospital
  • Vanderbilt University Medical Center
  • Sentara Heart Hospital
  • Madigan Army Medical Center

Outcomes

Primary Outcome Measures

Major amputation-free survival

Secondary Outcome Measures

Full Information

First Posted
July 17, 2007
Last Updated
August 19, 2008
Sponsor
FoxHollow Technologies
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1. Study Identification

Unique Protocol Identification Number
NCT00504088
Brief Title
Plaque Removal Versus Open Bypass Surgery For Critical Limb Ischemia
Acronym
PROOF
Official Title
Plaque Removal Versus Open Bypass Surgery For Critical Limb Ischemia
Study Type
Interventional

2. Study Status

Record Verification Date
August 2007
Overall Recruitment Status
Terminated
Why Stopped
Company decision to halt study
Study Start Date
October 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
FoxHollow Technologies

4. Oversight

5. Study Description

Brief Summary
To compare the outcome of bypass surgery and plaque excision for treatment of critical limb ischemia in the lower limbs

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Vascular Diseases
Keywords
CLI, Critical Limb Ischemia, PAD, Peripheral Arterial Disease, Artherosclerosis, Leg Pain, Cardiovascular, Artherectomy, Bypass, Peripheral Bypass, PROOF

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
Bypass
Intervention Type
Procedure
Intervention Name(s)
Silverhawk Plaque Excision
Primary Outcome Measure Information:
Title
Major amputation-free survival

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Ischemic rest pain for more than 2 weeks or ulceration or gangrene of the foot or toes (Rutherford Becker Category 4, 5 or 6) Willing and able, as evaluated by the PI, to provide Informed Consent Willing to undergo up to 5 years of clinical follow up visits as scheduled Angiographic pattern of infrainguinal disease that can be reasonably managed either by surgery or plaque excision in the first instance Reconstitution of at least one patent target tibial segment below the knee which provides run-off to the foot The patient must be >18 years of age Target lesion(s) is located at or below the level of the superficial femoral artery Target lesion(s) is >50% stenosed by quantitative vascular angiography Ability to take at least one of the following types of medications: anti- platelet or anti-thrombotic therapy Exclusion Criteria: Patient has cardiac or cardiovascular comorbidities that would make surgery inappropriate Patient has terminal or Stage 4 cancer Patient has extensive gangrene that requires both a Below-the-Knee amputation and a revascularization procedure Previous stent in the target lesion Active infection at planned incision site The patient is a pregnant woman The patient has significant suprainguinal or Common Femoral disease that can not be treated either prior to or during the index procedure Target Lesion is a Chronic Total Occlusion (CTO) that is greater than 15cm in length and has severe, continuous calcification
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James F. McKinsey, M.D.
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alabama, Birmingham
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35294
Country
United States
Facility Name
Los Angeles Cardiology/Good Samaritan
City
Los Angeles
State/Province
California
ZIP/Postal Code
90017
Country
United States
Facility Name
UC Davis Vascular Center
City
Sacramento
State/Province
California
ZIP/Postal Code
95817
Country
United States
Facility Name
San Francisco VA Medical Center
City
San Francisco
State/Province
California
ZIP/Postal Code
94121
Country
United States
Facility Name
Stanford University Medical Center/Palo Alto VA
City
Stanford
State/Province
California
ZIP/Postal Code
94306
Country
United States
Facility Name
Heart & Vascular Clinic of Northern Colorado
City
Fort Collins
State/Province
Colorado
ZIP/Postal Code
80523
Country
United States
Facility Name
Holmes Regional Medical Center
City
Melbourne
State/Province
Florida
ZIP/Postal Code
32901
Country
United States
Facility Name
Sacred Heart Hospital
City
Pensacola
State/Province
Florida
ZIP/Postal Code
32504
Country
United States
Facility Name
University of Chicago
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60637
Country
United States
Facility Name
Advocate Christ Medical Center
City
Oak Lawn
State/Province
Illinois
ZIP/Postal Code
60453
Country
United States
Facility Name
St. Vincent
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46260
Country
United States
Facility Name
Iowa Methodist Medical Center
City
Des Moines
State/Province
Iowa
ZIP/Postal Code
50309
Country
United States
Facility Name
Vascular Surgery Associates
City
Baton Rouge
State/Province
Louisiana
ZIP/Postal Code
70809
Country
United States
Facility Name
Beth Isreal (BIDMC)
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02215
Country
United States
Facility Name
St. Vincent Hospital
City
Worchester
State/Province
Massachusetts
ZIP/Postal Code
01608
Country
United States
Facility Name
William Beaumont/Southeast Surgical
City
Royal Oak
State/Province
Michigan
ZIP/Postal Code
48073
Country
United States
Facility Name
Providence Hospital
City
Southfield
State/Province
Michigan
ZIP/Postal Code
48075
Country
United States
Facility Name
University of Mississippi
City
Jackson
State/Province
Mississippi
ZIP/Postal Code
39216
Country
United States
Facility Name
Alegent Health Research Center
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68152
Country
United States
Facility Name
Hackensack University Medical Center
City
Hackensack
State/Province
New Jersey
ZIP/Postal Code
07601
Country
United States
Facility Name
New Mexico Heart Institute, PA
City
Albuquerque
State/Province
New Mexico
ZIP/Postal Code
87102
Country
United States
Facility Name
St. Vincent's Medical Center
City
New York
State/Province
New York
ZIP/Postal Code
10011
Country
United States
Facility Name
NY Weill Cornell Medical Center
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States
Facility Name
Columbia Presbyterian
City
New York
State/Province
New York
ZIP/Postal Code
10604
Country
United States
Facility Name
Duke University Medical Center
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27712
Country
United States
Facility Name
Cleveland VAMC
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Facility Name
Thomas Jefferson University Hospital
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
Facility Name
Rhode Island Hospital
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02903
Country
United States
Facility Name
Vanderbilt University Medical Center
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37232
Country
United States
Facility Name
Sentara Heart Hospital
City
Norfolk
State/Province
Virginia
ZIP/Postal Code
23507
Country
United States
Facility Name
Madigan Army Medical Center
City
Tacoma
State/Province
Washington
ZIP/Postal Code
98431
Country
United States

12. IPD Sharing Statement

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Plaque Removal Versus Open Bypass Surgery For Critical Limb Ischemia

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