Safety and Efficacy of Interventional Treatment Through Atherectomy to Improve Vascular Functions and Patency in Symptomatic Peripheral Artery Disease - Pilot Study
| Registry | NCT04092972, acronym SAVioR |
|---|---|
| Status | Unknown |
| Phase | Not applicable |
| Study type | Interventional; non randomized, parallel, masking: single, basic science |
| Enrollment | 30 (Estimated) |
| Sponsor | University Hospital, Essen (Other); collaborators: Straub Medical AG |
| Conditions | Peripheral Arterial Disease, Claudication, Intermittent |
| Interventions | Atherectomy, POBA and DCB (Other) |
| Dates | start 2019-01-01, primary completion 2021-07-28 (estimated), completion 2021-08-31 (estimated), first posted 2019-09-17, last updated 2021-01-25 |
| Locations | 1 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
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.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Atherectomy | Experimental | Other: Atherectomy | Atherectomy and drug-coated balloon (DCB) |
| Standard care | Active comparator | Other: POBA and DCB | Standard care with predilation (POBA) and DCB |
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
| Facility | City | Country | Status |
|---|---|---|---|
| University Hospital Essen | Essen, North Rhine-Westphalia | Germany | Recruiting |