Safety and Efficacy of Atherectomy on VasculaR Functions

NCT04092972 — Not applicable, Unknown, 30 participants, University Hospital, Essen

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Safety and Efficacy of Interventional Treatment Through Atherectomy to Improve Vascular Functions and Patency in Symptomatic Peripheral Artery Disease - Pilot Study

RegistryNCT04092972, acronym SAVioR
StatusUnknown
PhaseNot applicable
Study typeInterventional; non randomized, parallel, masking: single, basic science
Enrollment30 (Estimated)
SponsorUniversity Hospital, Essen (Other); collaborators: Straub Medical AG
ConditionsPeripheral Arterial Disease, Claudication, Intermittent
InterventionsAtherectomy, POBA and DCB (Other)
Datesstart 2019-01-01, primary completion 2021-07-28 (estimated), completion 2021-08-31 (estimated), first posted 2019-09-17, last updated 2021-01-25
Locations1 site in Germany

Related Papers Related Patents Related Grants Related Experts
All trials for Peripheral Arterial Disease All trials for Claudication, Intermittent All trials of Atherectomy All trials of POBA and DCB

-Summary

Interventional strategies aim to restore tissue perfusion. However, despite the simple reopening of a narrowed artery they affect endothelial function, perpetuating dysfunctional vascular homeostasis. PTA and atherectomy might alter the endothelial function but the mechanisms are incompletely understood. The primary goal of atherectomy is vessel preparation and improving compliance, which could aid in preserving vessel functions. Aim of this study is to determine safety, efficacy, patency and vessel functions in the femoropopliteal artery following atherectomy and DCB.

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+Arms and interventions

ArmTypeInterventionsDescription
AtherectomyExperimentalOther: AtherectomyAtherectomy and drug-coated balloon (DCB)
Standard careActive comparatorOther: POBA and DCBStandard care with predilation (POBA) and DCB
  • Atherectomy (Other): Straub Rotarex S atherectomy and drug-coated balloon DCB. Predilation of the lesion with a predefined ballon (180 sec, Passeo-18). Thus, no direct DCB will be conducted. All DCB lengths (40mm to 200 mm) and Diameters (3mm to 7mm) are eligible for the Trial as long as used in the superficial femoral artery (SFA).
  • POBA and DCB (Other): Standard predilation (POBA) and DCB. Predilation of the lesion with a predefined ballon (180 sec, Passeo-18). Thus, no direct DCB will be conducted. All DCB lengths (40mm to 200 mm) and Diameters (3mm to 7mm) are eligible for the Trial as long as used in the superficial femoral artery (SFA).

+Outcome measures

Primary outcomes

  • Treatment-Emerged Adverse Events [6 months Follow Up]: Incidence of Treatment-Emerged Adverse Events as assessed by angiography and adverse event assessment
  • Primary patency [6 months Follow Up]: determined through doppler ultrasound

Secondary outcomes

  • Bail-out stent rate [6 months Follow Up]: success of atherectomy in the SFA including the bail-out stenting rates
  • FMD local [6 months Follow Up]: Local endothelial function and vasomotion testing as determinded by FMD of the femoral artery
  • Vessel stiffness [6 months Follow Up]: Vascular stiffness determined through pulse wave velocity (PWV)
  • target lesion revascularization [6 months Follow Up]: freedom from Target Lesion Revascularization (FTLR) is defined as the Need for percutaneous or interventional revascularization
  • ABI (Ankle Brachial Index) [6 months Follow Up]: Ankle Brachial Index assessed by Doppler
  • Systemic endothelial function [6 months Follow Up]: Change of endothelial function, assessed by the change in the vasodilation after reactive hyperaemia of the brachial artery (flow-mediated dilation = FMD)
  • Change in Plaque burden [during baseline visit]: Change in plaque burden is measured by plaque volume change using intravascular ultrasound (IVUS)
  • Change in plaque characteristic [during baseline visit]: Change in plaque characteristic is quantified using virtual histology using intravascular ultrasound (IVUS)

+Eligibility

Sex: All, ages: 18 Years to 80 Years

Inclusion Criteria:

* Peripheral artery disease, lesions in the SFA and popliteal artery.
* Clinical diagnosis of chronic, symptomatic lower limb ischemia as defined by Rutherford 2, 3, or 4
* Planed peripheral intervention TASC A-D
* Subject must be between 18 and 85 years old
* Female of childbearing potential must have a negative pregnancy test within 10 days prior to index procedure and utilize reliable birth control until completion of the 12-month angiographic evaluation
* Vessel diameter ≥3.0 mm and ≤7.0 mm
* Willing to comply with the specified follow-up evaluation
* Written informed consent prior to any study procedures

Exclusion Criteria:

* Thrombolysis within 72 hours prior to the index procedure
* Aneurysm in the femoral artery or popliteal artery
* Concomitant hepatic insufficiency, deep venous thrombus, coagulation disorder or receiving immunosuppressant therapy
* Unstable angina pectoris at the time of the enrollment
* Recent myocardial infarction or stroke < 30 days prior to the index procedure
* Life expectancy less than 12 months
* Septicemia at the time of enrollment
* Known or suspected active infection at the time of the index procedure, excluding an infection of a lower extremity wound of the target limb
* Known or suspected allergies or contraindications to aspirin, clopidogrel or heparin Presence of other hemodynamically significant outflow lesions in the target limb requiring a planned surgical intervention or endovascular procedure within 30 days after the index procedure

+Locations (1)

FacilityCityCountryStatus
University Hospital EssenEssen, North Rhine-WestphaliaGermanyRecruiting

+Publications

  • Results publication: Rammos C, Manzke A, Lortz J, Messiha D, Petrikhovich O, Janosi RA, Steinmetz M, Rassaf T. Mechanical atherothrombectomy improves endothelial function through plaque burden reduction in PAD. Vasa. 2022 Nov;51(6):377-385. doi: 10.1024/0301-1526/a001034. Epub 2022 Oct 4. PMID 36193630

+Investigators