MedPath

French Registry of Acute Coronary Syndrome

Conditions
Acute Myocardial Infarction
Interventions
Other: Blood sample
Registration Number
NCT00673036
Lead Sponsor
Assistance Publique - Hôpitaux de Paris
Brief Summary

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

Detailed Description

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

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
3750
Inclusion Criteria
  • admission within the 48 hours after the occurence of acute myocardial infarction (AMI)
  • written informed consent for the DNA and serum databank
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Exclusion Criteria
  • AMI occured within the 48 hours after therapeutic intervention (bypass, coronary angioplasty or other chirurgical intervention)
  • diagnostic of AMI not confirmed
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
1Blood sampleAdults (female and male) with a acute coronary syndrome
Primary Outcome Measures
NameTimeMethod
All causes mortality at each follow-up period6 months, each year
Secondary Outcome Measures
NameTimeMethod
Cardiovascular mortality6 month, each year
Pharmacogenetic and cardiovascular genetic studies associated to clinical outcomes6 month each year
validation of guidelines across the country6 month, each year
Serum databank for evaluation of biomarkers in MI6 month each year

Trial Locations

Locations (1)

French Society of Cardiology

🇫🇷

Paris, France

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