Clinical Trials Directory

Trials / Completed

CompletedNCT02066740

EverFlex™ Self-expanding Peripheral Stent With Entrust™ Delivery System Clinical Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
34 (actual)
Sponsor
Medtronic Endovascular · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DEVICEEverFlex™ stent with Entrust™ delivery system

Timeline

Start date
2014-02-01
Primary completion
2014-07-01
Completion
2014-07-01
First posted
2014-02-19
Last updated
2019-03-01
Results posted
2015-09-16

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT02066740. Inclusion in this directory is not an endorsement.