Clinical Trials Directory

Trials / Completed

CompletedNCT03026465

Vessel Injury in Relation With Strut Thickness Assessed by OCT

Vessel Injury in Relation With Strut Thickness Assessed by OCT (VISTA): A Comparison of Vascular Injury Induced by a Polymer Free Sirolimus and Probucol Eluting Stent and a Biodegradable-polymer Biolimus-eluting Stent

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Fundacion Investigacion Interhospitalaria Cardiovascular · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The objective of the present study is to determine the relation between vascular injury induced by the stent and strut thickness.

Detailed description

Thinner struts produce less arterial injury after stent implantation.The objective of the present study is to determine the relation between vascular injury induced by the stent and strut thickness. Vessel injury after stent implantation will be evaluated with optical coherence tomography (OCT). Two stents platforms with different strut thickness (Coroflex ISAR 50 microns and Biomatrix 120 microns) will be compared.

Conditions

Interventions

TypeNameDescription
DEVICEPolymer-free stentPCI using a polymer-free dual-drug sirolimus- and probucol-eluting stent (Coroflex ISAR)
DEVICEBiodegradable-polymer stentPCI using a biodegradable-polymer biolimus-eluting stent (Biomatrix)

Timeline

Start date
2017-02-16
Primary completion
2018-07-27
Completion
2018-07-27
First posted
2017-01-20
Last updated
2019-08-21

Locations

3 sites across 1 country: Spain

Source: ClinicalTrials.gov record NCT03026465. Inclusion in this directory is not an endorsement.