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

About this trial
This is an interventional diagnostic trial for Critical Limb Ischemia
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
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
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
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