At a glance
ClinicalIndex Comparison RecordN/ACompleted· 34 enrolled
Drug / intervention
EverFlex™ stent with Entrust™ delivery systemdevice
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.
EverFlex™ Self-expanding Peripheral Stent With Entrust™ Delivery System Clinical Study
In Brief
A clinical study evaluating EverFlex™ stent with Entrust™ delivery system for Peripheral Arterial Diseases. Completed, enrolled 34 participants across 1 site.
Detailed Summary
The purpose of this study is to collect acute confirmatory data to evaluate technical success and acute safety of the EverFlex™ self-expanding peripheral stent with Entrust™ delivery system.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPeripheral Arterial Diseases
CountriesGermany
Collaborators--
Timeline
N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
Enrollment StartFeb 2014
First PostedFeb 2014
Primary CompletionJul 2014
TodayJul 2026
First PostedFeb 19, 2014
Enrollment StartFeb 1, 2014
Primary CompletionJul 1, 2014
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 12.4 years ago
Interventions
EverFlex™ stent with Entrust™ delivery systemdevice