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A Randomized Trial of Intracoronary Reopro to Improve Coronary Microvascular Function

U

University of Melbourne

Status

Unknown

Conditions

Coronary Artery Disease
Myocardial Infarction

Treatments

Drug: Abciximab

Study type

Interventional

Funder types

Other

Identifiers

NCT02105870
SVH 001

Details and patient eligibility

About

Microvascular dysfunction is a key determinant of pathogenesis and outcome in patients suffering an acute myocardial infarction.

The investigators hypothesise that treatment with intracoronary abciximab, a potent anti platelet agent, at the time of coronary stent insertion, will improve microvascular function.

Full description

The index of microcirculatory resistance (IMR), an invasive measure of coronary microvascular function, correlates with clinical outcomes in patients with stable angina and ST elevation myocardial infarction. The glycoprotein IIb/IIIa receptor inhibitor, abciximab, improves coronary microvascular function and reduces major cardiac adverse events in patients with acute coronary syndromes. This study will investigate whether an intracoronary bolus of abciximab in patients with non-ST elevation myocardial infarction decreases IMR and improves microvascular function.

Enrollment

40 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient with acute coronary syndromes

Exclusion criteria

  • Patient with untreated malignancy, disseminated malignancy, active inflammatory diseases, active infectious diseases patients unable to give informed consent Patients with STEMI

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

40 participants in 2 patient groups, including a placebo group

Intracoronary abciximab (Reopro)
Experimental group
Description:
Intracoronary abciximab (Reopro)
Treatment:
Drug: Abciximab
Control group
Placebo Comparator group
Description:
Intracoronary Reopro

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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