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

Completed

• Conditions: Myocardial Infarction; Acute Coronary Syndrome

• Registration Number: NCT01237418
• Lead Sponsor: French Cardiology Society

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.

Study Timeline

• Study Start: 2010-10
• Study First Submitted: 2010-11-08
• Study First Submitted QC: 2010-11-08
• Study First Posted: 2010-11-09
• Primary Completion: 2020-12-31
• Study Completion: 2020-12-31
• Status Verified: 2025-02
• Last Update Submitted: 2025-02-06
• Last Update Posted: 2025-02-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 4168

Inclusion Criteria

Not provided

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Survival	1 month	Compare survival in the hospital after admission in Intensive Care Unit in the manner of care

Secondary Outcome Measures

Name	Time	Method
Survival in long-term	10 years

Trial Locations

Locations (1)

European Hospital Georges Pompidou; 🇫🇷 Paris, France