Korea University Anam Hospital Optical Coherence Tomography Registry

November 14, 2016 updated by: Dr. Cheol Woong Yu, Korea University Anam Hospital

Optical Coherence Tomography Registry of Korea University Anam Hospital

All comer registry who had undergone intravascular optical coherence tomography during and/or after coronary intervention.

Study Overview

Detailed Description

Optical coherence tomography registry is composed with before coronary stenting, immediate after coronary stenting and follow-up study.

Study Type

Observational

Enrollment (Anticipated)

2000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Seoul, Korea, Republic of, 136-705
        • Recruiting
        • Korea University Anam Hospital
        • Contact:
          • Cheol Woong Yu, M.D., Ph.D.
          • Phone Number: +82-2-920-6726
          • Email: ycw717@naver.com

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

All comer registry with patients who had undergone coronary intervention and optical coherence tomography

Description

Inclusion Criteria:

  • patients who had undergone coronary intervention and optical coherence tomography

Exclusion Criteria:

  • none

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Optical Coherence Tomography registry group
Patients who had undergone optical coherence tomography within coronary intervention
Intracoronary imaging device which can precisely observe intracoronary structures

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Incidence of participants with Major Adverse Cardiovascular Events (MACE)
Time Frame: Up to 10 years
Composite of non-fatal myocardial infarction, all cause death, target vessel revascularization
Up to 10 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Do-Sun Lim, MD, PhD, Korea University Anam Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

April 1, 2016

Primary Completion (Anticipated)

December 1, 2019

Study Completion (Anticipated)

December 1, 2021

Study Registration Dates

First Submitted

April 25, 2016

First Submitted That Met QC Criteria

November 14, 2016

First Posted (Estimate)

November 17, 2016

Study Record Updates

Last Update Posted (Estimate)

November 17, 2016

Last Update Submitted That Met QC Criteria

November 14, 2016

Last Verified

November 1, 2016

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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