Ticagrelor Versus Clopidogrel in Left Ventricular Remodeling After ST-segment Elevation Myocardial Infarction

NCT02224534 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 326

Last updated 2016-11-15

No results posted yet for this study

Summary

The purpose of the study is to evaluate the novel role of ticagrelor to improve long-term LV remodeling following ST-segment elevation myocardial infarction.

Conditions

  • ST Elevation Myocardial Infarction

Interventions

DRUG

Ticagrelor

Ticagrelor 180 mg as a loading dose and 90 mg twice daily as a maintenance dose

DRUG

Clopidogrel

Clopidogrel 600 mg as a loading dose and 75 mg once daily as a maintenance dose.

Sponsors & Collaborators

  • Chinese PLA General Hospital

    collaborator OTHER
  • Chungnam National University Hospital

    collaborator OTHER
  • Pusan National University Yangsan Hospital

    collaborator OTHER
  • National University Heart Centre, Singapore

    collaborator OTHER
  • Ulsan University Hospital

    collaborator OTHER
  • Kyungpook National University Hospital

    collaborator OTHER
  • Samsung Changwon Hospital

    collaborator OTHER
  • Kyunghee University Medical Center

    collaborator OTHER
  • Chungbuk National University Hospital

    collaborator OTHER
  • Chonnam National University Hospital

    collaborator OTHER
  • Seoul National University Bundang Hospital

    collaborator OTHER
  • Gyeongsang National University Hospital

    lead OTHER

Principal Investigators

  • Yongwhi Park, MD., PhD. · Gyeongsang National University Hospital

  • Young-Hoon Jeong, MD.,PhD. · Gyeongsan National University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-10-31
Primary Completion
2017-06-30
Completion
2017-12-31

Countries

  • China
  • Singapore
  • South Korea

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 NCT02224534 on ClinicalTrials.gov