Clinical Trials Directory

Trials / Completed

CompletedNCT01297257

DELIVER Study: DELiverability of the Resolute Integrity Stent in All-Comer Vessels and Cross-OvER Stenting

Status
Completed
Phase
Study type
Observational
Enrollment
7,845 (actual)
Sponsor
Medtronic Vascular · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The primary objective of the DELIVER Study is to assess the deliverability of the Resolute Integrity Stent as primary stent or as a secondary cross-over stent following delivery failure of another stent type in real world patients.

Conditions

Interventions

TypeNameDescription
DEVICEStent implantationSingle arm, open label stent implantation

Timeline

Start date
2011-02-01
Primary completion
2012-10-01
Completion
2013-04-01
First posted
2011-02-16
Last updated
2014-03-06
Results posted
2014-03-06

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT01297257. Inclusion in this directory is not an endorsement.

DELIVER Study: DELiverability of the Resolute Integrity Stent in All-Comer Vessels and Cross-OvER Stenting (NCT01297257) · Clinical Trials Directory