Acute Myocardial Infarction Clinical Trial
Official title:
Prospective Randomized Controlled Clinical Study to Compare Tirofiban Intracoronary Bolus-Only vs Intravenous Bolus Plus Infusion in Patients With ST Elevation Myocardial Infarction Undergoing Primary Percutaneous Coronary Intervention
Verified date | March 2010 |
Source | Kosuyolu Heart Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | Turkey: Ethics Committee |
Study type | Interventional |
The aim of this randomized trial is to compare the efficacy of high dose tirofiban administered as either an intracoronary bolus alone or as an intravenous bolus followed by a maintenance infusion with respect to microvascular perfusion and long term left ventricular infarct size, volumes and function.
Status | Completed |
Enrollment | 49 |
Est. completion date | August 2009 |
Est. primary completion date | February 2009 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 25 Years to 75 Years |
Eligibility |
Inclusion Criteria: - Typical ongoing ischemic chest pain for longer than 30 minutes - ST segment elevation of 0,1 mV or greater in at least two contiguous leads or a new left bundle branch block on the initial ECG. Exclusion Criteria: - Cardiogenic shock and / or clinical instability - previous STEMI - Malignant life threatening diseases - Presence of an additional lesion causing more than 50% narrowing distal to the culprit lesion - Contraindications to aspirin, clopidogrel, or heparin - inability to give informed consent. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Kosuyolu Heart Hospital | The Society of Cardiac Health Protection |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Indices of microvascular perfusion | Intracoronary hemodynamic measures of index of microvascular resistance and coronary flow reserve | Post-PCI day 4 to 5 | No |
Secondary | ST segment resolution | post-PCI 90. minute | No | |
Secondary | corrected TIMI frame count | immediately after PCI, post-PCI day 4 to 5 | No | |
Secondary | Myocardial Blush Grade | immediately after PCI, post-PCI day 4 to 5 | No | |
Secondary | Scintigraphic infarct size | Left ventricular infarct size by SPECT | 6th month | No |
Secondary | Changes in left ventricular volume | Measured with echocardiography by using modified Simpson's method | Post-PCI day 3- 6th month | No |
Secondary | Composite of major adverse cardiovascular events | composite of reinfarction, target vessel revascularization and death. | 6 month | No |
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