patient with ST elevation myocardial acute infarction MedDRA version: 9.1 Level: SOC Classification code 10007541
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: patients with aged 18 years and 90 yearsa dmitted in hospital for acute coronary syndrome with persistente ST elevation and chest pain less than 12 hours Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range
Exclusion criteria
Exclusion criteria: shock cardiogenic, chronic dialisis, pregnancy, allergy to N-acetylcysteine, inability to obtain informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main Objective: determinate the effects of N-Acetytilcysteine versus placebo to prevent acute reduction in renal function after primary angioplasty;Secondary Objective: not avalable;Primary end point(s): assess the development of contrast induced acute renal failure | — |
Countries
Italy