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Comparing the effect of Loading Doses of Clopidogrel and Prasugrel on the incidence of myocardial injury in the Candidates for Elective Percutaneous Coronary Interventio

Phase 2
Conditions
Subsequent myocardial infarction.
For morbidity coding, this category should be assigned for infarction of any myocardial site, occurring within 4 weeks (28 days) from onset of a previous infarction
Registration Number
IRCT201408069768N3
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
90
Inclusion Criteria

we enrolled patients with stable angina who were candidate for elective PCI and gave informed consent to take part in this trial. The exclusion criteria included: history of coronary artery bypass graft surgery; need for emergency PCI (in less than 2 hours); history of renal dysfunction; any contraindication for prasugrel or Plavix; body weight<60 kg; age=75 years; history of cerebrovascular accident and transient ischemic attack, serum creatinine>1.5mg/dl; and ejection fraction<30%.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Periprocedural myocardial infarction. Timepoint: elevation of cTn values (>5 times) in patients with normal baseline values or a rise of cTn values >20% if the baseline values are elevated. Method of measurement: Blood survey.
Secondary Outcome Measures
NameTimeMethod
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