Ischemic Foot Ulcers: Is Intervention Better Than Wound Care Alone
Primary Purpose
Ischemic Foot Ulcer
Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Endovascular Revascularization
Sponsored by
About this trial
This is an interventional treatment trial for Ischemic Foot Ulcer focused on measuring Vascular
Eligibility Criteria
Inclusion Criteria:
- The subject (male or non-pregnant female) must be greater than or equal to 18 years of age
- Ischemic ulcer of foot present
- An ankle-brachial index (ABI) of 0.4 to 0.8 or monophasic-biphasic waveforms on pulse volume recordings. (If the subject is diabetic or has renal failure, with incompressible vessels, a toe brachial index of 0.4 to 0.8 is required.)
- Signed informed consent
Exclusion Criteria:
- Severe ischemia as defined by advanced gangrene, an ABI of less then or equal to 0.3 and monophasic waveforms on pulse volume recording
- Advanced renal insufficiency, defined as serum creatinine greater than or equal to 3 mg/dl
- Absolute contraindication to contrast media, as determined by the investigator
- Unwilling or unable to provide informed consent or return for required follow-up evaluations.
- Previous enrollment in this clinical study
- Concurrent participation in another clinical research study
Sites / Locations
- UPMC
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Active Comparator
Arm Label
Group I
Group 2
Arm Description
1. Wound Care (group 1)--Best standard wound care with aggressive debridement
2. Endovascular Intervention + Wound Care (group 2)--Best standard wound care in combination with endovascular revascularization Endovascular revascularization is the intervention
Outcomes
Primary Outcome Measures
Primary endpoint: wound healing at 4 weeks and 12 weeks
Secondary Outcome Measures
Secondary endpoints: amputation free survival, time to healing, quality of life, major adverse events.
Full Information
NCT ID
NCT00731835
First Posted
August 6, 2008
Last Updated
March 10, 2016
Sponsor
University of Pittsburgh
Collaborators
Society for Vascular Surgery
1. Study Identification
Unique Protocol Identification Number
NCT00731835
Brief Title
Ischemic Foot Ulcers: Is Intervention Better Than Wound Care Alone
Official Title
Ischemic Foot Ulcers: Is Intervention Better Than Wound Care Alone? A Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
March 2016
Overall Recruitment Status
Terminated
Why Stopped
slow enrollment
Study Start Date
July 2008 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
September 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pittsburgh
Collaborators
Society for Vascular Surgery
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
You are being asked to take part in this study because your doctor has determined that you have an ischemic foot ulcer. This research study will compare two approved standard of care treatment modalities for the management of ischemic foot ulcers. The ischemic foot ulcer (wound) on your foot is a result of a blocked artery in your leg. The wound can sometimes be healed with wound care alone, which includes dressing changes with creams and removing (debriding) the dead tissue. Alternatively, the significant narrowing or blockage in one of the arteries in your leg can be treated with several endovascular treatment techniques including:
angioplasty, also called percutaneous transluminal angioplasty (PTA) and/or
stent placement
atherectomy
The hypothesis of this study is that early endovascular or surgical intervention in subjects with moderate arterial insufficiency and a non-healing foot ulcer results in a higher overall incidence of wound healing in a significantly shorter period of time.
Detailed Description
Design:
This study is a single center, prospective, randomized trial evaluating the benefit of endovascular intervention on the healing of ischemic foot ulcers when compared to best wound care alone. The study population will be comprised of subjects with a foot ulcer and non-palpable or diminished pedal pulses. The expected duration of subjects in this trial is 2 years.
Patients will be randomized into two groups:
Wound Care (group 1)--Best standard wound care with aggressive debridement
Endovascular Intervention + Wound Care (group 2)--Best standard wound care in combination with endovascular revascularization
Subjects will undergo standard of care evaluation for ischemic foot ulcers. These same evaluations would be performed whether or not the subject was participating in this research study. In the event that a clinically significant event or unanticipated disease or condition is identified, the subject and their doctor will be notified, the investigator, will review the results of the tests and procedures that are standard of care, and the results will become part of the research record. Prior to undergoing randomization, the subject will sign and fully understand an IRB consent form that is HIPAA compliant.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemic Foot Ulcer
Keywords
Vascular
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
4 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Group I
Arm Type
No Intervention
Arm Description
1. Wound Care (group 1)--Best standard wound care with aggressive debridement
Arm Title
Group 2
Arm Type
Active Comparator
Arm Description
2. Endovascular Intervention + Wound Care (group 2)--Best standard wound care in combination with endovascular revascularization
Endovascular revascularization is the intervention
Intervention Type
Procedure
Intervention Name(s)
Endovascular Revascularization
Intervention Description
angioplasty, also called percutaneous transluminal angioplasty (PTA) and/or
stent placement
atherectomy
Primary Outcome Measure Information:
Title
Primary endpoint: wound healing at 4 weeks and 12 weeks
Time Frame
4 weeks and 12 weeks
Secondary Outcome Measure Information:
Title
Secondary endpoints: amputation free survival, time to healing, quality of life, major adverse events.
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
110 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
The subject (male or non-pregnant female) must be greater than or equal to 18 years of age
Ischemic ulcer of foot present
An ankle-brachial index (ABI) of 0.4 to 0.8 or monophasic-biphasic waveforms on pulse volume recordings. (If the subject is diabetic or has renal failure, with incompressible vessels, a toe brachial index of 0.4 to 0.8 is required.)
Signed informed consent
Exclusion Criteria:
Severe ischemia as defined by advanced gangrene, an ABI of less then or equal to 0.3 and monophasic waveforms on pulse volume recording
Advanced renal insufficiency, defined as serum creatinine greater than or equal to 3 mg/dl
Absolute contraindication to contrast media, as determined by the investigator
Unwilling or unable to provide informed consent or return for required follow-up evaluations.
Previous enrollment in this clinical study
Concurrent participation in another clinical research study
Facility Information:
Facility Name
UPMC
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15232
Country
United States
12. IPD Sharing Statement
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Ischemic Foot Ulcers: Is Intervention Better Than Wound Care Alone
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