MedTrace Logo

Vessel Injury in Relation With Strut Thickness Assessed by OCT

NCT03026465 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2019-08-21

No results posted yet for this study

Summary

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

Conditions

Interventions

DEVICE

Polymer-free stent

PCI using a polymer-free dual-drug sirolimus- and probucol-eluting stent (Coroflex ISAR)

DEVICE

Biodegradable-polymer stent

PCI using a biodegradable-polymer biolimus-eluting stent (Biomatrix)

Sponsors & Collaborators

  • B.Braun Surgical SA

    collaborator INDUSTRY

  • Fundacion Investigacion Interhospitalaria Cardiovascular

    lead OTHER

Principal Investigators

  • Nieves Gonzalo, MD, PhD · Hospital Clinico San Carlos de Madrid

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-02-16
Primary Completion
2018-07-27
Completion
2018-07-27

Countries

  • Spain

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03026465 on ClinicalTrials.gov