search
Back to results

Matrix Metalloproteinases in Patients With Critical Limb Ischemia Undergoing Surgical Revascularization (ROMAMETA)

Primary Purpose

Critical Limb Ischemia, Extracellular Matrix Alteration, Peripheral Revascularisation

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Polytetrafluoroethylene (PTFE) bypass grafting.
Autogenous vein bypass grafting
Sponsored by
University of Catanzaro
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Critical Limb Ischemia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • patients with CLI stage III-IV according to the Fontaine's classification

Exclusion Criteria:

  • Patients with evidence of systemic sepsis, known neoplastic disease or any established generalized inflammatory disease

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Experimental

    Arm Label

    Group I

    Group II

    Arm Description

    Intervention: Polytetrafluoroethylene (PTFE) bypass grafting.

    Intervention: Autogenous vein bypass grafting.

    Outcomes

    Primary Outcome Measures

    MMPs evaluation
    MMPs plasma levels will be evaluated during follow up.

    Secondary Outcome Measures

    Full Information

    First Posted
    March 9, 2015
    Last Updated
    March 13, 2015
    Sponsor
    University of Catanzaro
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT02388867
    Brief Title
    Matrix Metalloproteinases in Patients With Critical Limb Ischemia Undergoing Surgical Revascularization
    Acronym
    ROMAMETA
    Official Title
    Predictive Role of Matrix Metalloproteinases for the Outcome of Surgical Revascularization in Patients With Critical Limb Ischemia
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2015
    Overall Recruitment Status
    Completed
    Study Start Date
    January 2012 (undefined)
    Primary Completion Date
    January 2015 (Actual)
    Study Completion Date
    March 2015 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Catanzaro

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    In the present study the investigators will evaluate MMPs. serum levels variations in patients affected by critical limb ischemia, before and after lower limb surgical revascularization through venous or prosthetic bypass.
    Detailed Description
    Recent clinical studies showed an association between Peripheral Artery Disease (PAD) and circulating levels of Matrix Metalloproteinases (MMPs), especially MMP-2, MMP-9, MMP-8 and MMP-10, compared with healthy controls. A recent study showed the association between MMP-10 serum levels and severity and poor outcome in patients affected by Critical Limb Ischemia (CLI). Also, MMPs seems to be involved in intimal hyperplasia and constrictive remodeling, both responsible of restenosis after surgical treatment of atherosclerotic lesions. Intimal hyperplasia is a thickening of the tunica intima resulting in narrowing of the vessel lumen. Elevated tissue levels of MMP-2 and MMP-9 have been identified in pig models of vein bypass grafts, temporally coinciding with the period of Smooth Muscle Cells (SMC) migration and neointimal formation. In the present study the investigators want to evaluate MMP-1; MMP-2, MMP-9, MMP-8 and MMP-10 serum levels variations in patients affected CLI, before and after lower limb surgical revascularization through venous or prosthetic bypass in order to assess their role in predicting the surgical outcome of these procedures. Patients with CLI will be randomized to receive lower limb surgical revascularization through autogenous venous (Group I) or prosthetic bypass (using synthetic polytetrafluoroethylene - PTFE- ) (Group II). Patients enrolled in the present study will be followed through clinical and ultrasonographic examination at 1, 3, 6, 12 and 24 months. At the same time points MMPs plasma levels (by means of blood sampling through venipuncture) will be evaluated. Clinical, Instrumental and Laboratory data then will be matched.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Critical Limb Ischemia, Extracellular Matrix Alteration, Peripheral Revascularisation

    7. Study Design

    Primary Purpose
    Diagnostic
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    30 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Group I
    Arm Type
    Experimental
    Arm Description
    Intervention: Polytetrafluoroethylene (PTFE) bypass grafting.
    Arm Title
    Group II
    Arm Type
    Experimental
    Arm Description
    Intervention: Autogenous vein bypass grafting.
    Intervention Type
    Procedure
    Intervention Name(s)
    Polytetrafluoroethylene (PTFE) bypass grafting.
    Intervention Description
    Polytetrafluoroethylene (PTFE) bypass grafting. Patients will undergo bypass procedure using PTFE graft : the inflow vessel may be the femoral artery or the iliac artery; the outflow vessel may be the popliteal artery or the anterior tibial artery.
    Intervention Type
    Procedure
    Intervention Name(s)
    Autogenous vein bypass grafting
    Intervention Description
    Autogenous vein bypass grafting. Patients will undergo Bypass procedure using autogenous veins (the great saphenous vein or the small saphenous vein or a composite bypass using great and small saphenous vein ). The inflow vessel may be represented by the femoral artery or the popliteal artery; the outflow vessel may be the anterior tibial artery or the posterior tibial artery or the peroneal artery.
    Primary Outcome Measure Information:
    Title
    MMPs evaluation
    Description
    MMPs plasma levels will be evaluated during follow up.
    Time Frame
    24 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: patients with CLI stage III-IV according to the Fontaine's classification Exclusion Criteria: Patients with evidence of systemic sepsis, known neoplastic disease or any established generalized inflammatory disease

    12. IPD Sharing Statement

    Learn more about this trial

    Matrix Metalloproteinases in Patients With Critical Limb Ischemia Undergoing Surgical Revascularization

    We'll reach out to this number within 24 hrs