A Safety and Efficacy Study of the Dynalink®-E Everolimus Eluting Peripheral Stent System
- Conditions
- AtherosclerosisPeripheral Vascular Disease
- Interventions
- Device: Dynalink®-E everolimus-eluting peripheral stentDevice: Dynalink®-E, everolimus-eluting peripheral stent
- Registration Number
- NCT00475566
- Lead Sponsor
- Abbott Medical Devices
- Brief Summary
The purpose of this first-in-man study is to evaluate the safety and performance of the Dynalink®-E everolimus eluting peripheral stent system for the treatment of patients with atherosclerotic de novo or restenotic native superficial femoral and proximal popliteal lesions.
Abbott Vascular is ceasing data analysis of the STRIDES Clinical Trial after 2 years. The decision to discontinue the study is not related to any safety concern. The rationale for this proposal is based on the following considerations:
The performance of DYNALINK-E from STRIDES shows no device- or procedure-related deaths and no stent fractures, and the rate of additional revascularizations has been stable since approximately 14 months after the procedure.
Evaluations of the bare metal nitinol DYNALINK and ABSOLUTE stents in the clinical literature show low rates of death, reintervention and stent fracture, which are consistent with STRIDES and demonstrate the safety of the nitinol stent platform of the DYNALINK-E.
Long-term animal studies show no concerns with the drug or polymer coating of DYNALINK-E - everolimus tissue concentration drops below the quantifiable limit by approximately 17 months after implant, and vascular response to the coating is normal with widely patent lumens and struts incorporated into vessel tissue.
The safety and performance of the DYNALINK-E has been substantiated by its clinical and pre-clinical data, and by the clinical data of similar products. Given the demonstrated mechanical integrity of the stent along with the evidence of a healthy long-term vascular response, there is a reasonable expectation of continued low event rates.
- Detailed Description
A prospective, Non-Randomized, Single-arm, Multi-center, Clinical Study to Evaluate the Safety and Performance of the Dynalink®-E, Everolimus Eluting Peripheral Stent System for the Treatment of Atherosclerotic de Novo or Restenotic Native Superficial Femoral and Proximal Popliteal Artery Lesions.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 104
- Rutherford Becker Category 2-5
- Single de novo or restenotic lesion in the superficial femoral or proximal popliteal artery
- Disease segment length 30-170 mm
- >50% diameter stenosis or total occlusion
- Target reference vessel diameter 4.3-7.3 mm
- Target lesion previously treated with stent or surgery
- Rutherford Becker Category 0, 1, or 6
- Immunosuppressive disorder or currently receiving immunosuppressive agents
- Serum creatinine >2.5 mg/dl
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description 1 Dynalink®-E everolimus-eluting peripheral stent This is a prospective, non-randomized, single-arm, multi-center study. A projected 100 patients will receive the stent(s) in this study at approximately 10-15 European sites. The primary objective is to evaluate the safety and performance of the Dynalink®-E everolimus eluting peripheral stent system for the treatment of patients with atherosclerotic de novo or restenotic native superficial femoral or proximal popliteal lesions. 1 Dynalink®-E, everolimus-eluting peripheral stent This is a prospective, non-randomized, single-arm, multi-center study. A projected 100 patients will receive the stent(s) in this study at approximately 10-15 European sites. The primary objective is to evaluate the safety and performance of the Dynalink®-E everolimus eluting peripheral stent system for the treatment of patients with atherosclerotic de novo or restenotic native superficial femoral or proximal popliteal lesions.
- Primary Outcome Measures
Name Time Method In-stent binary restenosis (>50% stenosis), as measured by duplex ultrasound 6 months
- Secondary Outcome Measures
Name Time Method Angiographic in-stent binary restenosis rate (>50%) 12 months Angiographic mean in-stent late loss, in-stent mean minimum lumen diameter (MLD), percent diameter stenosis 12 months Primary, and secondary patency 1, 6, 12, 18 months, 2, 3, 4, 5 years
Trial Locations
- Locations (10)
Landeskrankenhaus Klagenfurt
🇦🇹Klagenfurt, Austria
Allgemeines Krankenhaus der Stadt Wien- AKH Wien
🇦🇹Wien, Austria
Sint Blasius Hospital
🇧🇪Dendermonde, Belgium
ZOL St. Jan
🇧🇪Gent, Belgium
University Hospital
🇧🇪Gent, Belgium
University Hospital Tübingen
🇩🇪Tübingen, Germany
Herzzentrum Leipzig
🇩🇪Leipzig, Germany
Herzzentrum Bad Krozingen
🇩🇪Bad Krozingen, Germany
The Jewish Hospital Berlin
🇩🇪Berlin, Germany
Casa di Cura di Montevergine
🇮🇹Mercogliano, Italy