French Registry of Acute Coronary Syndrome

Assistance Publique - Hôpitaux de Paris3,750 enrolled

Overview

The Fast-MI registry was designed to evaluate the "real world" management of patients with acute myocardial infarction (MI), and to assess their in-hospital, medium and long-term outcomes

Primary objectives : compare survival following the admission to a USIC according to the terms of care

Study Type

OBSERVATIONAL

Enrollment

3,750

Conditions

Acute Myocardial Infarction

Interventions

Blood sampleOTHER

60 ml of whole blood

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * admission within the 48 hours after the occurence of acute myocardial infarction (AMI) * written informed consent for the DNA and serum databank Exclusion Criteria: * AMI occured within the 48 hours after therapeutic intervention (bypass, coronary angioplasty or other chirurgical intervention) * diagnostic of AMI not confirmed

Locations (1)

French Society of Cardiology

Paris, France

Outcomes

Primary Outcomes

All causes mortality at each follow-up period

Time frame: 6 months, each year

Secondary Outcomes

Cardiovascular mortality

Time frame: 6 month, each year

validation of guidelines across the country

Time frame: 6 month, each year

Pharmacogenetic and cardiovascular genetic studies associated to clinical outcomes

Time frame: 6 month each year

Serum databank for evaluation of biomarkers in MI

Time frame: 6 month each year

Data from ClinicalTrials.gov

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