Endovascular treatment of symptomatic atherosclerotic peripheral artery disease (PAD) is recommended as the primary revascularization strategy. Percutaneous transluminal angioplasty (PTA) of the superficial femoral artery has a high initial success rate, but restenosis and dissections frequently occur.The influence of the novel devices with improved hemodynamic capabilities with respect to vasomotion of the vessel wall, vascular function and vascular compliance can be measured by FMD (flow-mediated dilation), arterial stiffness indices and vascular strain analysis. The aim of this ITT is to determine the potential improvement and impact of the SELUTION SLR in the infrainguinal arteries on local vascular function.
Endovascular treatment of symptomatic atherosclerotic peripheral artery disease (PAD) is recommended as the primary revascularization strategy. Percutaneous transluminal angioplasty (PTA) of the superficial femoral artery has a high initial success rate, but restenosis and dissections frequently occur. While restoration of tissue perfusion is achieved, these interventional strategies affect vascular function, perpetuating dysfunctional vascular homeostasis. Vascular and endothelial dysfunction per se is the pathophysiologic principle involved in the initiation and progression of atherosclerosis and has been correlated to higher incidences of cardiac events such as myocardial infarction or the need for interventions. PTA and DCB treatment alter the endothelial homeostasis but the impact and detailed mechanisms are incompletely understood. The influence of the novel devices with improved hemodynamic capabilities with respect to vasomotion of the vessel wall, vascular function and vascular compliance can be measured by FMD (flow-mediated dilation), arterial stiffness indices and vascular strain analysis. The aim of this ITT is to determine the potential improvement and impact of the SELUTION SLR in the infrainguinal arteries on local vascular function. Device to be used are SELUTION SLR™ (Sustained Limus Release) drug eluting balloon (n = 35) vs. Active comparator, Paclitaxel eluting balloon (Medtronic InPact, n = 35) The analysis of the primary end point will be performed on an intention-to-treat basis. Subgroup analyses will be performed according to PAD classification etiology and based on stent length.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
70
Sirolimus DCB
Paclitaxel DCB
University of Essen, Clinic of Cardiology and Angiology
Essen, North Rhine-Westphalia, Germany
RECRUITINGChange of flow-mediated vasodilation (FMD) of the nonstenotic segment of the proximal SFA after procedure
FMD represents the percent diameter gain as calculated based on preischemia and postischemia diameter measurements of the femoral artery
Time frame: 1 month
Change of flow-mediated vasodilation (FMD) of the nonstenotic segment of the proximal SFA after procedure
FMD represents the percent diameter gain as calculated based on preischemia and postischemia diameter measurements of the femoral artery
Time frame: 6 months
Change of flow-mediated vasodilation (FMD) of the nonstenotic segment of the proximal SFA after procedure
FMD represents the percent diameter gain as calculated based on preischemia and postischemia diameter measurements of the femoral artery
Time frame: 12 months
Changes in pulse wave velocity (PWV)
Changes in cardiovascular function measured by pulse wave velocity in m/s
Time frame: Baseline, followed at 1, 6 and 12 months
Changes in augmentation index
Changes in cardiovascular function measured by augmentation index in %
Time frame: Baseline, followed at 1, 6 and 12 months
Changes in vascular strain
Changes in cardiovascular function measured by vascular strain in %
Time frame: Baseline, followed at 1, 6 and 12 months
Changes in peripheral perfusion determined by ABI (ankle brachial index)
ABI measurements are conducted using a Doppler probe on tibial and anterior artery locations. The highest value will be used for calculation and divided by the highest systolic brachial Doppler pressure
Time frame: Baseline, followed at 1, 6 and 12 months
Primary patency (PP) of target lesion
Primary patency determined by PVR measurement with ultrasound
Time frame: Baseline, followed at 1, 6 and 12 months
Changes in clinical symptoms
Clinical symptoms of patients determined by Walking impairment questionaire (WIQ)
Time frame: Baseline, followed at 1, 6 and 12 months
Changes in six-minute walk test
Six-minute walk test determined by pain-free walking distance in m
Time frame: Baseline, followed at 1, 6 and 12 months
Procedural complications
Any procedural complications
Time frame: Baseline, followed at 1, 6 and 12 months
Freedom from Target Lesion Revascularization
Freedom from Target Lesion Revascularization (FTLR)
Time frame: Baseline, followed at 1, 6 and 12 months
MALE
Any unplanned vascular event and minor or major amputations
Time frame: Baseline, followed at 1, 6 and 12 months
Changes of inflammatory profile measured by hs-CRP in mg/dl
Blood samples are collected at the below mentioned time points
Time frame: Baseline, followed at 1, 6 and 12 months
Changes of inflammatory profile measured by oxLDL in µg/l
Blood samples are collected at the below mentioned time points
Time frame: Baseline, followed at 1, 6 and 12 months
Changes of inflammatory profile measured by Interleukin-6 in pg/ml
Blood samples are collected at the below mentioned time points
Time frame: Baseline, followed at 1, 6 and 12 months
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