ISRCTN56034553CompletedNot Applicable
PREVEC Trial: Prevention of Reperfusion damage associated with percutaneous coronary angioplasty following acute myocardial infarction: a randomized double-blind placebo-controlled clinical trial
Scientific and Technological Development Fund (FONDECYT Fondo de Desarrollo Científico y Tecnológico) (Chile)0 sites132 target enrollmentStarted: January 28, 2013Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 132
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •1. Subjects may be of either sex and must be at least 18 years old
- •2. Subjects must have indication of primary percutaneous coronary angioplasty (PCA) as follows:
- •2.1. Angina or equivalent at least 120 min duration
- •2.2. Electrocardiogram (ECG) with STEMI that concerns more than 2 contiguous leads (>2mm)
- •3. Presentation within 12 h of symptoms onset
- •4. First myocardial infarction
- •5. Subject must be able and willing to sign informed consent
Exclusion Criteria
- •1. History of renal or hepatic insufficiency
- •2. History of renal lithiasis (oxalates)
- •3. History of heart failure (NYHA III, IV)
- •4. Cardiogenic shock
- •5. Any serious medical co-morbidity that determine life expectancy < 6 month
- •6. Current participation in any other clinical investigation
- •7. Pregnancy
- •8. Glucose 6-phosphate dehydrogenase deficiency
Investigators
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