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Vascular Healing of DES at 3 Months

NCT01391871 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 46

Last updated 2013-08-02

No results posted yet for this study

Summary

The purpose of this study is to compare vascular healing of the stented segment after deployment of new PRO-Kinetic drug eluting stent and Endeavor Resolute zotarolimus-eluting stent in patients with acute coronary syndromes requiring percutaneous coronary intervention.

Conditions

  • Acute Coronary Syndrome

Interventions

DEVICE

OCT

Optical coherence tomography

DEVICE

Transthoracic echocardiography CFR measurement

CFR will be assessed using transthoracic echocardiography with adenosine infusion.

Sponsors & Collaborators

  • The Hospital District of Satakunta

    collaborator OTHER

  • University of Turku

    lead OTHER

Principal Investigators

  • Tuomas Kiviniemi, MD, PhD · Turku University Hospital

  • Pasi Karjalainen, MD, PhD · Satakunta Central Hospital

  • Antti Ylitalo, MD, PhD · Satakunta Central Hospital

  • Juhani Airaksinen, MD, PhD, FESC · Turku University Hospital

Eligibility

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

Timeline & Regulatory

Start
2011-06-30
Primary Completion
2012-07-31
Completion
2013-07-31

Countries

  • Finland

Study Locations

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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 NCT01391871 on ClinicalTrials.gov