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BIONICS 38 mm Trial EluNIR Ridaforolimus Eluting Coronary Stent System (EluNIR) In Coronary Stenosis Trial
This is a prospective, multi-center, single-arm, open-label clinical trial. Clinical follow-up will be performed at 30 days. Follow-up by phone will be performed at 6 months, and 1 year after the procedure. Study Objective is to further assess the safety and efficacy of long (38 mm) Ridaforolimus Eluting Stent - EluNIR.
Details
| Lead sponsor | Medinol Ltd. |
|---|---|
| Phase | NA |
| Status | COMPLETED |
| Enrolment | 50 |
| Start date | Wed Nov 14 2018 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Thu Apr 30 2020 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Coronary Stenosis
Interventions
- EluNIR Ridaforolimus Eluting Coronary Stent System
Countries
Israel