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Abbreviated Antithrombotic Therapy After PCI in Patients With AF and AMI (HERO-AF-AMI)

30 de agosto de 2026 actualizado por: Young Joon Hong, Chonnam National University Hospital

Heart-team for Evidence-based RevascularizatiOn: Abbreviated Antithrombotic Therapy After Percutaneous Coronary Intervention in Patients With Atrial Fibrillation and Acute Myocardial Infarction

The aim of the study is to compare clinical outcomes between direct oral anticoagulant (DOAC) monotherapy versus dual antithrombotic therapy (DOAC plus clopidogrel) in patients with atrial fibrillation and acute myocardial infarction after percutaneous coronary intervention (PCI).

Descripción general del estudio

Descripción detallada

Advancements in device technologies for PCI and adjunct pharmacotherapy have recently shifted research focus toward balancing bleeding risk reduction with the management of ischemic events through novel antithrombotic strategies. These trends are particularly relevant for patients with atrial fibrillation (AF) who require lifelong oral anticoagulation to prevent embolic events. Traditionally, the combination of vitamin K antagonists (such as warfarin) with antiplatelet agents has been regarded as the standard approach to mitigate ischemic risk following PCI in patients with AF. However, previous studies have consistently demonstrated that dual antithrombotic therapy (DAT) utilizing direct oral anticoagulants (DOACs) results in reduced bleeding complications compared to triple antithrombotic therapy based on warfarin.

For long-term maintenance, DOAC monotherapy is recommended, as a Class I, after 6 to 12 months post-PCI for patients with stable coronary artery disease (CAD) and AF. Recent randomized clinical trials corroborate these recommendations. The AFIRE (Atrial Fibrillation and Ischemic Events with Rivaroxaban in Patients with Stable Coronary Artery Disease) study showed that rivaroxaban monotherapy was non-inferior to DAT in terms of both bleeding and ischemic outcomes. The EPIC-CAD (Edoxaban versus Edoxaban with Antiplatelet Agent in Patients with Atrial Fibrillation and Chronic Stable Coronary Artery Disease) trial further extended this evidence, indicating that edoxaban monotherapy reduced the risk of net adverse clinical events (NACE)-a composite of death, myocardial infarction, stroke, systemic embolism, unplanned urgent revascularization, and major or clinically relevant nonmajor bleeding-compared to DAT. Recently, the ADAPT AF-DES (Appropriate Duration of Antiplatelet and Thrombotic Strategy after 12 Months in Patients with Atrial Fibrillation Treated with Drug-Eluting Stents) trial demonstrated that DOAC monotherapy was non-inferior, and even superior, to combination therapy with a DOAC and clopidogrel regarding NACE reduction in patients with AF and stable CAD following PCI. However, these studies have primarily focused on patients with stable CAD who inherently have a lower ischemic risk. Despite limited evidence supporting DOAC monotherapy as a maintenance strategy for acute myocardial infarction (AMI) patients, recent guidelines have also recommended this approach after 1 year (Class I) or 6 months (Class IIB) following PCI in AMI setting. Furthermore, in real-world data, the DAT remained effective in reducing ischemic events without increasing the risk of bleeding compared with DOAC monotherapy. Additionally, DOAC monotherapy showed a lower risk of NACE at 3 years, but was not significantly effective at 1 year after PCI.

To address this critical evidence gap in clinical practice, we have developed the Heart-team for Evidence-based Revascularization: Abbreviated Antithrombotic Therapy After Percutaneous Coronary Intervention in Patients with Atrial Fibrillation and Acute Myocardial Infarction (HERO-AF-AMI). This study aims to evaluate the impact of DOAC monotherapy compared to DAT (DOAC plus clopidogrel) in patients with AF and AMI undergoing PCI.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

860

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Seung Hun Lee, MD, PhD
  • Número de teléfono: 82-2-220-6246
  • Correo electrónico: lsh8602@naver.com

Copia de seguridad de contactos de estudio

  • Nombre: Joon Ho Ahn, MD, PhD
  • Número de teléfono: 82-2-220-6246
  • Correo electrónico: yhbky@naver.com

Ubicaciones de estudio

    • Gwangju
      • Gwangju, Gwangju, Corea del Sur, 61469
        • Reclutamiento
        • Chonnam National University Hospital
        • Sub-Investigador:
          • Seung Hun Lee, MD, PhD
        • Investigador principal:
          • Young Joon Hong, MD, PhD
        • Sub-Investigador:
          • Joon Ho Ahn, MD, PhD
        • Contacto:
          • Young Joon Hong, MD, PhD
          • Número de teléfono: 82-62-220-6246
          • Correo electrónico: hyj200@hanmail.net
        • Contacto:
          • Seung Hun Lee, MD, PhD
        • Sub-Investigador:
          • Seok Oh, MD, PhD

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  1. Patients aged 19 years old
  2. Patients with AF and CHA2DS2-VA score ≥2.
  3. ST-segment elevation myocardial infarction (STEMI) or Non-ST-segment elevation myocardial infarction (NSTEMI)

    • STEMI: ST-segment elevation ≥0.1 mV in ≥2 contiguous leads or documented newly developed left bundle-branch block.12
    • NSTEMI: NSTEMI is defined as a combination of criteria with mandated elevation of a cardiac biomarker, preferably high-sensitive cardiac troponin with at least one value above 99th percentile of the upper reference limit and at least one of the following:12

      1. Symptoms of ischemia.
      2. New or presumed new significant ST-T wave changes
      3. Development of pathological Q waves on electrocardiography.
      4. Imaging evidence of new or presumed new loss of viable myocardium or regional wall motion abnormality.
      5. Intracoronary thrombus detected on angiography.
  4. Patients underwent PCI for AMI (STEMI or NSTEMI) at least 6 months before enrollment.

Exclusion Criteria:

  1. Patients contraindicated for use of DOACs or clopidogrel
  2. Mechanical prosthetic valve or moderate-to-severe mitral stenosis requiring vitamin K antagonist
  3. Planned cardiac surgery within 1 year after randomization
  4. Patients with severe thrombocytopenia or coagulopathy
  5. Liver cirrhosis or severe hepatic dysfunction
  6. Advanced chronic kidney disease (creatinine clearance <15 ml/min/1.73 m2) or on dialysis
  7. Prior history of intracranial hemorrhage
  8. Coexisting conditions related to high risk of life-threatening bleeding
  9. Pregnancy or breast feeding
  10. Non-cardiac co-morbid conditions are present with life expectancy <1 year or that may result in protocol non-compliance (per site investigator's medical judgment)
  11. Unwillingness or inability to comply with the procedures described in this protocol.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Comparador activo: DAT (DOAC+clopidogrel) group
Patients who were indicated lifelong oral anticoagulation for AF with a CHA2DS2-VA score equal to or greater than 2 points, and treated AMI with PCI are candidates. After 6 months of index procedure, the patients will be screened for inclusion and exclusion criteria, and eligible patients will be randomized into either the DOAC monotherapy group or the DAT group. Patients allocated to the DAT group receive either apixaban 5 mg twice daily, edoxaban 60 mg once daily, or rivaroxaban 15 mg once daily with clopidogrel 75 mg once daily.
Patients allocated to the DAT group receive either apixaban 5 mg twice daily, edoxaban 60 mg once daily, or rivaroxaban 15 mg once daily with clopidogrel 75 mg once daily.
Experimental: DOAC monotherapy group
Patients who were indicated lifelong oral anticoagulation for AF with a CHA2DS2-VA score equal to or greater than 2 points, and treated AMI with PCI are candidates. After 6 months of index procedure, the patients will be screened for inclusion and exclusion criteria, and eligible patients will be randomized into either the DOAC monotherapy group or the DAT group. Patients allocated to the DOAC monotherapy group receive either apixaban 5 mg twice daily, edoxaban 60 mg once daily, or rivaroxaban 20 mg once daily.
Patients allocated to the DOAC monotherapy group receive either apixaban 5 mg twice daily, edoxaban 60 mg once daily, or rivaroxaban 20 mg once daily.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
NACE (net adverse clinical events)
Periodo de tiempo: 1 year after the last patient enrollment
a composite of death, non-fatal MI, stroke, systemic embolization, unplanned revascularization, stent thrombosis, major or clinically relevant non-major bleeding by ISTH
1 year after the last patient enrollment

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Rate of major bleeding by ISTH
Periodo de tiempo: 1 year after the last patient enrollment
major bleeding events by ISTH definition
1 year after the last patient enrollment
Rate of MACCE (major adverse cardiac and cerebrovascular event)
Periodo de tiempo: 1 year after the last patient enrollment
a composite of cardiovascular death, non-fatal MI, ischemic stroke, systemic embolization, unplanned revascularization, and stent thrombosis
1 year after the last patient enrollment
All-cause death
Periodo de tiempo: 1 year after the last patient enrollment
all-cause death
1 year after the last patient enrollment
Cardiovascular death
Periodo de tiempo: 1 year after the last patient enrollment
cardiovascular death
1 year after the last patient enrollment
Rate of non-fatal MI
Periodo de tiempo: 1 year after the last patient enrollment
non-fatal MI, defined by Fourth Universal definition of MI
1 year after the last patient enrollment
Rate of ischemic stroke
Periodo de tiempo: 1 year after the last patient enrollment
ischemic stroke
1 year after the last patient enrollment
Rate of systemic embolization
Periodo de tiempo: 1 year after the last patient enrollment
systemic embolization
1 year after the last patient enrollment
Rate of unplanned revascularization
Periodo de tiempo: 1 year after the last patient enrollment
unplanned revascularization (clinically-driven)
1 year after the last patient enrollment
Rate of definite stent thrombosis
Periodo de tiempo: 1 year after the last patient enrollment
definite stent thrombosis, defined by Academic Research Consortium (ARC) II consensus
1 year after the last patient enrollment
Rate of cardiovascular death or non-fatal MI
Periodo de tiempo: 1 year after the last patient enrollment
a composite of cardiovascular death or non-fatal MI
1 year after the last patient enrollment
Rate of all-cause death, non-fatal MI, stroke, systemic embolization, stent thrombosis, or ISTH major bleeding
Periodo de tiempo: 1 year after the last patient enrollment
a composite of all-cause death, non-fatal MI, stroke, systemic embolization, stent thrombosis, or ISTH major bleeding
1 year after the last patient enrollment
Rate of major or clinically relevant non-major bleeding by ISTH
Periodo de tiempo: 1 year after the last patient enrollment
major or clinically relevant non-major bleeding by ISTH
1 year after the last patient enrollment
Rate of fatal bleeding by ISTH
Periodo de tiempo: 1 year after the last patient enrollment
fatal bleeding by ISTH
1 year after the last patient enrollment
Rate of clinically relevant non-major bleeding by ISTH
Periodo de tiempo: 1 year after the last patient enrollment
clinically relevant non-major bleeding by ISTH
1 year after the last patient enrollment
Rate of any bleeding by ISTH
Periodo de tiempo: 1 year after the last patient enrollment
any bleeding by ISTH
1 year after the last patient enrollment

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Blood pressure control status
Periodo de tiempo: 1 year after the last patient enrollment
mean value, variability, and control rate of blood pressure
1 year after the last patient enrollment
AF rhythm event
Periodo de tiempo: 1 year after the last patient enrollment
AF episode frequency and lasting time
1 year after the last patient enrollment
AF burden (%)
Periodo de tiempo: 1 year after the last patient enrollment
AF burden (%)
1 year after the last patient enrollment

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Silla de estudio: Young Joon Hong, MD, PhD, Chonnam National University

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

26 de agosto de 2026

Finalización primaria (Estimado)

31 de diciembre de 2031

Finalización del estudio (Estimado)

31 de diciembre de 2032

Fechas de registro del estudio

Enviado por primera vez

7 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

7 de mayo de 2026

Publicado por primera vez (Actual)

13 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

2 de septiembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

30 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

SÍ

Descripción del plan IPD

After publication of main paper, de-identified data will be shared upon reasonable requests after discussion by Executive Committee.

Marco de tiempo para compartir IPD

After publication of main paper.

Criterios de acceso compartido de IPD

Executive Committee will discuss to share the de-identified data upon reasonable requests.

Tipo de información de apoyo para compartir IPD

  • PROTOCOLO DE ESTUDIO
  • SAVIA
  • RSC

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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