Comparison of Two Lower Limb Bypass Types : Prosthesis Versus Autologous Vein (REVA)
Primary Purpose
Arteritis, Diabetes
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
femoropopliteal artery bypass
femoropopliteal artery bypass
Sponsored by
About this trial
This is an interventional treatment trial for Arteritis focused on measuring arteritis, lower limb ischemia, femoropopliteal artery bypass, blood vessel prothesis implantation, saphenous vein, vascular permeability, doppler ultrasonography, randomized clinical trials, efficacy study
Eligibility Criteria
Inclusion Criteria: lower limbs arteritis : II to IV arteritis level, above knee femoro popliteal bypass indication signed informed consent Exclusion Criteria: no contra indication to the use of prosthesis Available saphenous vein no major trophic trouble
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
1
2
Arm Description
bypass by autologous saphenous vein
bypass by dacron or PTFE Prosthesis
Outcomes
Primary Outcome Measures
Bypass permeability 5 years after surgery, assessed trough Doppler ultrasonography
Secondary Outcome Measures
Mortality
Morbidity
permeability predictive factors (smoking habits, diabetes, hyperlipidemia, bypass diameter)
Primary and secondary permeability
leg salvage
Full Information
NCT ID
NCT00221715
First Posted
September 13, 2005
Last Updated
May 7, 2013
Sponsor
University Hospital, Bordeaux
Collaborators
Ministry of Health, France
1. Study Identification
Unique Protocol Identification Number
NCT00221715
Brief Title
Comparison of Two Lower Limb Bypass Types : Prosthesis Versus Autologous Vein
Acronym
REVA
Official Title
Randomised Study Comparing Prosthesis and Autologous Vein for Revascularisation With Above Knee Femoropopliteal Bypass.
Study Type
Interventional
2. Study Status
Record Verification Date
May 2013
Overall Recruitment Status
Completed
Study Start Date
July 2002 (undefined)
Primary Completion Date
May 2011 (Actual)
Study Completion Date
May 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Bordeaux
Collaborators
Ministry of Health, France
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
When medical treatments fail, critical ischemia of the lower limb often leads to surgery, i.e. above knee femoro popliteal bypass. This bypass can be performed either with DACRON or PTFE prosthesis or with the autologous saphenous vein. Both technics are used but they have not been compared regarding bypass permeability and limb salvage. Thus, this study will compare the permeability rate of above knee femoro popliteal surgery whether performed with autologous vein versus prosthesis
Detailed Description
When medical treatments fail, critical ischemia of the lower limb often leads to surgery, i.e. above knee femoro popliteal bypass. This bypass can be performed with either DACRON or PTFE prosthesis or with the autologous saphenous vein. The principle disadvantages of prosthesis are their prejudged worse permeability and the risk of infection. Too few reliable randomised, multicentric studies in this indication comparing vein bypasses versus prosthesis bypasses have been conducted to firmly confirm the first argument. Thus, the purpose of this multicentric, randomised, national study is to compare, 5 years after surgery, the permeability rate of above knee femoropopliteal bypass with vein versus prosthesis. Primary and secondary permeability, permeability predictive factors, and leg salvage rate will also be assessed. One hundred enrolled patients with II to IV level leg arteritis will randomly be assigned to one of the surgery groups : vein or prosthesis (50 each). The recruiting period will last 3 years and a half, and the follow up 5 years for each patient. The main primary outcome, bypass permeability, will be assessed through Doppler ultrasonography during five years. Secondary endpoints, mortality and morbidity, will be evaluated during the clinical follow up. Permeability predictive factors, primary and secondary permeability, leg salvage will also be recorded. If the permeability rates are equivalent between prosthesis and vein, the use of prosthesis will be preferred as this surgery is easier and faster, and as it is important that the vein remains available for distal revascularisation (where it is more efficient) and for revascularisation of coronary arteries
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Arteritis, Diabetes
Keywords
arteritis, lower limb ischemia, femoropopliteal artery bypass, blood vessel prothesis implantation, saphenous vein, vascular permeability, doppler ultrasonography, randomized clinical trials, efficacy study
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
100 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
bypass by autologous saphenous vein
Arm Title
2
Arm Type
Active Comparator
Arm Description
bypass by dacron or PTFE Prosthesis
Intervention Type
Device
Intervention Name(s)
femoropopliteal artery bypass
Intervention Description
Bypass by autologous saphenous vein
Intervention Type
Device
Intervention Name(s)
femoropopliteal artery bypass
Intervention Description
bypass by dacron or PTFE Prosthesis
Primary Outcome Measure Information:
Title
Bypass permeability 5 years after surgery, assessed trough Doppler ultrasonography
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Mortality
Time Frame
5 years
Title
Morbidity
Time Frame
5 years
Title
permeability predictive factors (smoking habits, diabetes, hyperlipidemia, bypass diameter)
Time Frame
5 years
Title
Primary and secondary permeability
Time Frame
5 years
Title
leg salvage
Time Frame
5 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
lower limbs arteritis : II to IV arteritis level, above knee femoro popliteal bypass indication
signed informed consent
Exclusion Criteria:
no contra indication to the use of prosthesis
Available saphenous vein
no major trophic trouble
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dominique Midy, Professor
Organizational Affiliation
University Hospital, Bordeaux
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Geneviève Chêne, Professor
Organizational Affiliation
University Hospital, Bordeaux
Official's Role
Study Chair
12. IPD Sharing Statement
Learn more about this trial
Comparison of Two Lower Limb Bypass Types : Prosthesis Versus Autologous Vein
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