The goal of primary PCI is to restore anterograde myocardial flow. Stenting a largely
thrombotic lesion may determine distal embolisation of thrombotic material therefore
deteriorating myocardial perfusion.
Procedure: Immediate stenting
Procedure: Delayed stenting
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Locations near you
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Full eligibility criteria for NCT01462188
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
chest pain for >30 min with ST-segment elevation of one mm or more in 2 or more contiguous ECG leads or with presumably new left bundle-branch block
admission either within 12 h of symptom onset or between 12 and 24 h with evidence of continuing ischaemia
the exclusion criteria will include history of bleeding diathesis or documented allergy/intolerance or contraindication to clopidogrel or ticlopidine or prasugrel
inability to assume an oral P2Y12 receptor blocker on a consecutive daily basis for a minimum of 6 months, or to heparin or aspirin
uncontrolled hypertension (systolic or diastolic arterial pressure >180 mmHg or 120, respectively, despite medical therapy)
limited life expectancy, e.g. neoplasms, others
inability to obtain informed consent
patients were not enrolled if they were clinically unstable, presented with severe arrhythmia, or had known contraindications to CMR (claustrophobia, pacemakers, or implantable defibrillator devices)
All locations for NCT01462188
Ferrara, Emilia Romagna, Italy, 44100
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View full eligibility
Tris trial is registered with FDA with number: NCT01462188. The sponsor of the trial is Marco Valgimigli and it is looking for 100 volunteers for the current phase.
Official trial title: Immediate Versus Delayed Stenting in Patients With ST-Elevation Myocardial Infarction Undergoing Mechanical Intervention
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