CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 775 enrolled
Drug / intervention
Peripheral stentingdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02921230
NCT02921230N/ACompleted

A Randomized Trial Comparing the ELUVIA Drug-eluting Stent Versus Bare Metal Self-expanding Nitinol Stents in the Treatment of Superficial Femoral and/or Proximal Popliteal Arteries

Boston Scientific Corporation·interventional·Posted Oct 3, 2016·Updated Feb 24, 2025

In Brief

A clinical study evaluating Peripheral stenting for Arterial Occlusive Diseases and 3 related conditions. Completed, enrolled 775 participants across 60 sites in 10 countries.

Detailed Summary

The EMINENT study is a prospective, multi-center study evaluating the effectiveness of the ELUVIA stent versus Self-Expanding Bare Nitinol Stents in the treatment of lesions in the femoropopliteal arteries.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustria, Belgium, France, Germany, Ireland, Italy, Netherlands, Spain, Switzerland, United Kingdom
Collaborators--

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedOct 3, 2016
Enrollment StartOct 25, 2016
Primary CompletionJul 2, 2021
Study CompletionNov 6, 2023
TodayJul 2, 2026
Enrollment to primary: 4.7 yearsPosted 9.7 years ago

Interventions

Peripheral stentingdevice

stent implantation during the index procedure