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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
University Hospital, Bordeaux
About
Eligibility
Locations
Arms
Outcomes
Full info

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

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

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

    First Posted
    September 13, 2005
    Last Updated
    May 7, 2013
    Sponsor
    University Hospital, Bordeaux
    Collaborators
    Ministry of Health, France
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    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

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    Comparison of Two Lower Limb Bypass Types : Prosthesis Versus Autologous Vein

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