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The effect of vitamin C on acute MI in primary PCI setting

Not Applicable
Conditions
acute myocardial infarction.
Acute transmural myocardial infarction of unspecified site
Registration Number
IRCT201606048698N19
Lead Sponsor
Vice chancellor for research, Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
320
Inclusion Criteria

inclusion criteria:
Subjects (men or women) at least 18 years and less than 80 years of age; Ischemic discomfort =20 minutes and =6 hours of duration;
ST elevation =1mm (=0.1mV) in two contiguous limb leads OR =2mm (=0.2mV) in two contiguous precordial leads; Planned primary PCI within 2 hours of hospital presentation; Planned or concomitant use of aspirin, clopidogrel, unfractionated heparin, and Glycoprotein IIb/IIIa inhibition with intent to stent the infarct-related artery; Informed consent able to be obtaine

Exclusion Criteria

Age =80 years; Cardiac arrest or arrhythmia requiring chest compressions or cardiopulmonary resuscitation; Current warfarin therapy; Known allergy or contraindication to fibrinolytics OR aspirin OR heparin OR clopidogrel; Patients with evidence of coronary collaterals (2-3 Rentrop) to the region at risk on previous coronary angiography (at the previous admission) .

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Myocardial infarction. Timepoint: before intervention. Method of measurement: clinical history and ECG.;Myocardial perfusion grade. Timepoint: after PCI. Method of measurement: by angiographic interpretation.;TIMI flow. Timepoint: after stenting. Method of measurement: by angiographic interpretation.;P selectin kit. Timepoint: one month. Method of measurement: ELISA.
Secondary Outcome Measures
NameTimeMethod
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