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French Registry of Acute Coronary Syndrome With or Without ST Elevation 2010

French Registry of Acute Coronary Syndrome With or Without ST Elevation 2010

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01237418
Acronym
FAST-MI 2010
Enrollment
4168
Registered
2010-11-09
Start date
2010-10-31
Completion date
2020-12-31
Last updated
2025-02-10

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

Conditions

Acute Coronary Syndrome, Myocardial Infarction

Brief summary

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.

Detailed 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.

Interventions

None listed

Sponsors

French Cardiology Society
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

: * 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

Design outcomes

Primary

MeasureTime frameDescription
Survival1 monthCompare survival in the hospital after admission in Intensive Care Unit in the manner of care

Secondary

MeasureTime frame
Survival in long-term10 years

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026