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French Registry of Acute Coronary Syndrome

French Registry of Acute Coronary Syndrome With or Without ST Elevation

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00673036
Acronym
Fast-MI
Enrollment
3750
Registered
2008-05-07
Start date
2005-10-31
Completion date
2019-06-30
Last updated
2017-01-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Myocardial Infarction

Keywords

Coronary syndrome, Myocardial infarction, French registry

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

Interventions

OTHERBlood sample

60 ml of whole blood

Sponsors

French Cardiology Society
CollaboratorOTHER
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
All causes mortality at each follow-up period6 months, each year

Secondary

MeasureTime frame
Cardiovascular mortality6 month, each year
validation of guidelines across the country6 month, each year
Pharmacogenetic and cardiovascular genetic studies associated to clinical outcomes6 month each year
Serum databank for evaluation of biomarkers in MI6 month each year

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 4, 2026