Ticagrelor in Patients With ST Elevation Myocardial Infarction Treated With Pharmacological Thrombolysis

NCT02298088 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 3799

Last updated 2019-02-15

No results posted yet for this study

Summary

Administration of Ticagrelor in patients with ST elevation myocardial infarction treated with pharmacological thrombolysis

Conditions

  • Acute ST Segment Elevation Myocardial Infarction
  • Thrombolysis in Myocardial Infarction Flow

Interventions

DRUG

Ticagrelor 180 mg

Ticagrelor, 180 mg as early as possible after the index event and not \>24 h post event followed by 90 mg twice daily for 12 months.

DRUG

Clopidogrel

300 mg clopidogrel as early as possible after the index event and not \> 24h post event, followed by 75mg/day for 12 months. For patients with \> 75 years the recommended load dose is 75 mg instead 300 mg.

Sponsors & Collaborators

  • Hospital do Coracao

    lead OTHER

Principal Investigators

  • Otavio Berwanger, MD,PhD · Hospital do Coracao

  • Helio P Guimaraes, MD,PhD · Hospital do Coracao

  • Leopoldo S Piegas, MD,PhD · Hospital do Coracao

  • Renato D Lopes, MD,PhD · Duke University

  • Jose C Nicolau, MD,PhD · Instituto do Coracao HC-FMUSP

  • Francisco A Fonseca, MD,PhD · Universidade Federal de São Paulo

  • Jose F Saraiva, MD,PhD · Hospital e Maternidade Celso Pierro

  • Carlos Tajer, MD,PhD · Investigación Independiente S.A.

  • Stephen Nicholls, MD,PhD · South Australian Health and Medical Research Institute

  • Shaun Goodman, MD,PhD · Canadian Heart Research Centre

  • Lixin Jiang, MD,PhD · Chinese Academy of Medical Sciences, Fuwai Hospital

  • Harvey White, MD,PhD · Auckland City Hospital - Auckland District Health Board

  • Germán Malaga, MD,PhD · Universidad Peruana Cayetano Heredia

  • Oleg Averkov, MD,PhD · Clinical Hospital #15 Clinical Hospital #15 named after O.M.Filatov, Moscow, Russia

  • Alexander Parkhomenko, MD,PhD · Institute of Cardiology - Emergency Cardiology Department

  • Christopher Granger, MD,PhD · Duke University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2015-08-31
Primary Completion
2017-12-31
Completion
2019-01-31

Countries

  • Argentina
  • Australia
  • Brazil
  • Canada
  • China
  • Colombia
  • New Zealand
  • Peru
  • Russia
  • Ukraine

Study Locations

More Related Trials

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 NCT02298088 on ClinicalTrials.gov