Current partner codePEPTIDESDE
NCT00251823·Phase 3·INTERVENTIONAL

Safety and Efficacy Study of Eptifibatide in Primary Percutaneous Coronary Intervention (PCI)

Status

Completed

Phase

Phase 3

Enrollment

400

Locations

1

Results

Not posted

Publications

1

Study summary

What the protocol is testing.

Rationale: ST-elevation myocardial infarction (STEMI) is usually triggered by rupture of an atherosclerotic plaque that then accumulates platelets and fibrin and leads to an occlusive coronary thrombus. Clinical benefits obtained with revascularization of the infarct related artery (IRA) depend on the achievement of four goals: 1. Early reperfusion 2. Full restoration of normal flow in the epicardial vessels 3. Full restoration of flow in the microcirculation, and 4. Preservation of myocardial function. Reperfusion of the IRA can be achieved pharmacologically with intravenous thrombolytic agents, or mechanically with percutaneous coronary intervention (PCI). In Canada, thrombolysis is the current standard of care in most hospitals, although there is mounting evidence that primary PCI is superior, and many Canadian centres are shifting towards this strategy. To offer primary PCI to community hospitals without on site cardiac catheterization facilities, regional programs need to be present that allow rapid transfer to invasive centers that offer this procedure round-the-clock. Recent evidence suggests that angiographic and clinical results with primary PCI could be further enhanced by facilitation with a pharmacological treatment given prior to the procedure. The present proposal plans to examine the safety and efficacy of eptifibatide to facilitate coronary angioplasty in STEMI in patients who present to centres with and without on-site catheterization facilities. The primary outcome measure will be a composite clinical endpoint including death, recurrent myocardial infarction, recurrent unstable ischemia, or stroke, at 30 days. Secondary endpoints include the percent thrombolysis in myocardial infarction (TIMI) grade 3 coronary flow after the PCI, myocardial perfusion score, individual clinical outcomes as listed for the primary endpoint, resolution of ST-segment elevation, requirement for subsequent revascularization, frequency of congestive heart failure (CHF), cardiogenic shock, and Canadian Cardiovascular Society (CCS) angina class.

Interventions

Treatment arms and agents.

DRUG

Eptifibatide facilitated PCI

Timeline

From registration to results.

  1. First posted

    Nov 10, 2005

  2. Study start

    Jul 2005

  3. Primary completion

    Not reported

  4. Study completion

    Sep 2008

  5. Results posted

    Not reported

  6. Registry updated

    Sep 4, 2008

Outcomes

What the study measures.

Primary outcomes

The primary clinical endpoint is a composite measure of clinical outcomes of death, recurrent myocardial infarction, and recurrent severe ischemia, which will be assessed at 30 days after the index acute myocardial infarction (AMI)

Secondary outcomes

Determine if a facilitated PCI strategy with early initiation of eptifibatide improves the percentage of patients with TIMI grade 3 flow measured at the time of baseline angiography

improves post procedural TIMI perfusion scoreC

improves ST-segment elevation resolution, a surrogate marker of clinical efficacy

improves left ventricular (LV) ejection fraction

improves functional capacity

decreases subsequent revascularization (PCI , or coronary artery bypass graft [CABG])

Eligibility

Who can take part.

Minimum age
Not reported
Maximum age
Not reported
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: * Ischemic chest discomfort of 30 minutes duration * Onset of chest pain 12 hours prior to entry into the study * ST segment elevation of \> 1 mm (0.1 mV) in two or more contiguous electrocardiographic leads (on a standard 12 lead electrocardiogram \[ECG\]), or left bundle branch block not known to be old Exclusion Criteria: * Active bleeding * History of stroke within 90 days or any intracranial bleed. * Major surgery or trauma within the past 6 weeks * Uncontrolled hypertension (systolic blood pressure \[SBP\] 200 mm Hg and/or diastolic blood pressure \[DBP\] 110 mm Hg despite treatment) * Prolonged (\> 10 minutes) cardiopulmonary resuscitation * Inadequate vascular access * PCI within the last 30 days * Thrombolytic agents within the preceding 7 days * Concurrent use of warfarin * A blood coagulation disorder (i.e. international normalized ratio \[INR\] \> 2.0, platelet count \< 100,000/mm3, or hematocrit \< 30%) * Intolerance to aspirin or clopidogrel * A subcutaneous therapeutic dose of any low molecular weight heparin (LMWH) within 12 hours * Known severe contrast allergy * Other medical condition that is likely to result in death within 12 months * Participation in a study or another investigational device or drug trial within the past four weeks * Pregnancy * Known severe renal impairment (creatinine \> 200 mole/l) * Sustained hypotension, systolic blood pressure \< 80 mm Hg, or the need for intravenous (IV) inotropes and/or intraaortic balloon counterpulsation to support the blood pressure * Inability to provide informed consent

Study locations

1 registered sites.

Canada. Showing up to 24 locations stored in the fast local snapshot.

University of Ottawa Heart Institute

Ottawa, Ontario, Canada

Related trials

More studies on Eptifibatide.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.