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COMPARE-II- Vasomotion and Imaging Substudy

NCT01329237 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2011-04-05

No results posted yet for this study

Summary

The purpose of the study is to compare strut coverage and neointimal thickness between everolimus eluting (XIENCE-V® or PROMUS® stent) and biolimus A9 eluting NOBORI Stent 14 months after stent implantation and to determine the coronary endothelial function after everolimus eluting (XIENCE-V® or PROMUS® stent) and biolimus A9 eluting NOBORI Stent 14 months after stent implantation by using supine bicycle exercise testing to assess coronary vasomotor response to exercise.

Conditions

Interventions

OTHER

dynamic physical exercise and OCT imaging

supine dynamic physical exercise during coronary angiography and optical coherence tomography OCT imaging of the coronary stent

Sponsors & Collaborators

  • University of Freiburg

    lead OTHER

Principal Investigators

  • Mario Togni, MD · University of Fribourg, Switzerland

  • Stéphane Cook, MD · University of Fribourg, Switzerland

  • Jean-Christophe Stauffer, MD · Hopital Cantonal HFR, Fribourg, Switzerland

  • Jean-Jacques Goy, MD · Hopital Cantonal HFR, Fribourg, Switzerland

  • Gérard Baeriswyl, MD · Hopital Cantonal HFR, Fribourg, Switzerland

  • Pieter C Smits, MD, PhD · Maasstad Ziekenhuis, Rotterdam, The Netherlands

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-03-31
Primary Completion
2012-03-31

Countries

  • Switzerland

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 NCT01329237 on ClinicalTrials.gov