This trial is active, not recruiting.

Conditions myocardial infarction, acute coronary syndrome
Sponsor French Cardiology Society
Start date October 2010
End date December 2021
Trial size 3700 participants
Trial identifier NCT01237418, 10240


The observatory FAST MI 2010 proposes to establish a cohort of 3500 patients recruited prospectively over a period of 2 months.

Patients will be followed up at 1 month and then followed annually for 10 years.

Patients should have agreed to participate in the study, participation in the protocol, or refusal to participate will not affect the therapeutic approach of the physician. The study of genotypic or phenotypic characteristics will not change the therapeutic approach of health care teams.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Observational model cohort
Time perspective prospective
Any patient over 18 years admitted for myocardial infarction (MI) of less than 48 hours, characterized by the typical rise and fall of troponin or CPKMb

Primary Outcomes

time frame: 1 month

Secondary Outcomes

Survival in long-term
time frame: 10 years

Eligibility Criteria

Male or female participants at least 18 years old.

Inclusion Criteria : - Patients over 18 years old - Admitted patient for a myocardial infarction (MI) of less than 48 hours, characterized by the typical rise and fall of troponin or CPKMb associated with at least one of the following: symptoms of myocardial ischemia or appearance of pathological Q waves or repolarization disorders related to ischemia (in addition to or NSTEMI) - Patient who consented to participate in the study Exclusion Criteria: - Refusal of consent - MI occurring within 48 h after a therapeutic intervention (angioplasty or coronary bypass or other surgery) - Diagnosis of SCA reversed in favor of an alternative diagnosis

Additional Information

Official title French Registry of Acute Coronary Syndrome With or Without ST Elevation 2010
Principal investigator Nicoals Danchin
Description This is a multicenter observational study, given to 300 prospective medical facilities, CHU, CHG, CHR, health facility of the Army, including a clinic or intensive care unit entitled to receive emergency ACS. (See attached list 10-6) A questionnaire will be sent to each center before the recruitment center on the type and number of beds (Appendix 10-5) Patients will be recruited consecutively in the CIAU member during a period of 2 months. The 1-month follow-up will be done by the referring physician of each ISB, by mail or telephone contact with the treating physician and / or patient. Annual follow-ups will be conducted during 10 years of clinical research technicians of the French Society of Cardiology, mail and / or telephone contact with the municipalities of birth, treating physicians and patients.
Trial information was received from ClinicalTrials.gov and was last updated in September 2013.
Information provided to ClinicalTrials.gov by French Cardiology Society.