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Bivalirudin/Prasugrel Versus Abciximab/Clopidogrel in Patients Presenting With STEMI

I

I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio

Status and phase

Unknown
Phase 4

Conditions

ST-Elevation Myocardial Infarction
Primary Percutaneous Coronary Intervention

Treatments

Drug: prasugrel/bivalirudin
Drug: clopidogrel/abciximab

Study type

Interventional

Funder types

Other

Identifiers

NCT01158846
Biva/Pra versus Abcix/clop (Registry Identifier)
B/P vs A/C for STEMI (Registry Identifier)

Details and patient eligibility

About

In the setting of ST elevation myocardial infarction newer therapies has been recently studied and, following encouraging results, introduced into the clinical practice. Prasugrel showed to be a valid alternative to overcome limitation of clopidogrel therefore providing a better ischemic protection. On the other hand, bivalirudin is at least as beneficial as heparin/abciximab as anticoagulant agent but associated with fewer hemorrhagic events. The primary hypothesis of the study is that the combination of prasugrel plus bivalirudin can be associated with a better risk/benefit profile.

Full description

Background:

In the setting of STEMI, adjunctive pharmacological therapy plays a key role in the acute management. Along with the clear benefit of mechanical reperfusion strategies, several drugs showed to be beneficial. On top of clopidogrel, heparins and IIB/IIIa glycoprotein, other drugs have been recently introduced showing encouraging results. These "new" drugs, namely prasugrel and bivalirudin, have only been compared separately.

Primary hypothesis: the combination of prasugrel/bivalirudin is superior to the combination of clopidogrel and heparin/abciximab in terms of net adverse clinical events, i.e. ischemic events plus hemorrhagic events

Setting:

  • patients presenting with ST-elevation myocardial infarction undergoing primary PCI

Mechanical reperfusion:

-primary percutaneous coronary intervention

Pharmacological Interventions:

  • Two arms: Clopidogrel plus heparin/abciximab vs Prasugrel plus Bivalirudin

Follow up:

  • 1 year

Measurements:

  • efficacy end points in terms of reduction of ischemic events
  • safety end points in terms of reduction of bleeding events

Enrollment

800 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ST elevation myocardial infarction
  • No contraindication to primary PCI

Exclusion criteria

  • Known intolerance/allergy to one of the study drugs or their components
  • Clinical indication to treatment with oral anticoagulant, including use of warfarin or dabigatran or other oral anticoagulant agents

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

800 participants in 2 patient groups

prasugrel/bivalirudin
Active Comparator group
Description:
60 mg loading dose of prasugrel will be followed by maintenance dose of 10mg (or 5mg according to body weight and age). During primary PCI, Bivalirudin will be used as anticoagulant (bolus plus infusion), on a weight-adjusted dose.
Treatment:
Drug: prasugrel/bivalirudin
clopidogrel/abciximab
Active Comparator group
Description:
600mg loading dose of clopidogrel will be followed by 75mg maintenance dose. During primary PCI abciximab (bolus plus infusion) will be used as anticoagulant.
Treatment:
Drug: clopidogrel/abciximab

Trial contacts and locations

1

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Central trial contact

Luca Testa, MD, PhD

Data sourced from clinicaltrials.gov

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