Genotyping Influences Outcome of Coronary Artery Stenting (GENIUS)

March 11, 2016 updated by: Do-sun Lim, Korea University Anam Hospital

Prospective Multi-center Registry of Genotyping Related Clopidogrel in Percutaneous Coronary Intervention Patients

This study evaluated epidemiology and clinical outcome of clopidogrel related various genotyping in Korean patients who had undergone percutaneous coronary intervention as a all comer registry form.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

This study evaluates the relationship between clopidogrel related various genotyping, epidemiology and clinical outcome of patient who had undergone percutaneous coronary intervention. Clopidogrel resistance was measured with VerifyNow, which is a device that can monitor platelet inhibition of clopidogrel. Genes which are known to be related with clopidogrel resistance were evaluated; (1-3) CYP 2C19 *2, *3, *17, (4) PON1 Q192R, (5) ABCB1 3435C->T, (6) P2Y12, (7) CYP 2C9 *3.

Study Type

Interventional

Enrollment (Actual)

5000

Phase

  • Not Applicable

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

20 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Written informed consent
  • Older than 20 years
  • All percutaneous coronary intervention patients within 1 month

Exclusion Criteria:

  • Pregnancy
  • Life expectancy below 1 year
  • Known aspirin or clopidogrel allergy

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

  • Primary Purpose: Diagnostic
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: GENIUS
All comer patients who had undergone percutaneous coronary intervention with administration of conventional dual anti-platelet treatment (aspirin 100mg and clopidogrel 75mg daily) for minimum 3 months
Administration of conventional dual anti-platelet treatment (aspirin 100mg and clopidogrel 75mg daily) for minimum 3 months after percutaneous coronary intervention
Other Names:
  • clopidogrel hydrogen sulfate 97.875mg (75mg as clopidogrel)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Myocardial infarction and Death
Time Frame: 1 year after index procedure
1 year after index procedure

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Any death
Time Frame: 1 year after index procedure
1 year after index procedure
Cardiac death
Time Frame: 1 year after index procedure
1 year after index procedure
Myocardial infarction
Time Frame: 1 year after index procedure
1 year after index procedure
Stent thrombosis (acute, late, very late)
Time Frame: 1 year after index procedure
1 year after index procedure
Target lesion revascularization
Time Frame: 1 year after index procedure
Revascularization of in-stent restenosis which developed in previously implanted stent on index procedure
1 year after index procedure
Stroke
Time Frame: 1 year after index procedure
Ischemic or hemorrhagic cerebral infarction diagnosed by brain MRI which developed within 1 year after index procedure
1 year after index procedure
Bleeding complication
Time Frame: During index procedure
During index procedure
PRU
Time Frame: Within index procedure
Value which is measured with VerifyNow that can monitor platelet inhibition of clopidogrel
Within index procedure
ARU
Time Frame: Within index procedure
Value which is measured with VerifyNow that can monitor platelet inhibition of aspirin
Within index procedure

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Do-sun Lim, MD, PhD, Cardiovascular center, Korea University Anam Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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

September 1, 2011

Primary Completion (Actual)

February 1, 2016

Study Completion (Actual)

February 1, 2016

Study Registration Dates

First Submitted

February 23, 2016

First Submitted That Met QC Criteria

March 11, 2016

First Posted (Estimate)

March 14, 2016

Study Record Updates

Last Update Posted (Estimate)

March 14, 2016

Last Update Submitted That Met QC Criteria

March 11, 2016

Last Verified

March 1, 2016

More Information

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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