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Clinical Trials/NCT01237418
NCT01237418
Completed
Not Applicable

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

French Cardiology Society1 site in 1 country4,168 target enrollmentStarted: October 2010Last updated:

Overview

Phase
Not Applicable
Status
Completed
Sponsor
French Cardiology Society
Enrollment
4,168
Locations
1
Primary Endpoint
Survival

Overview

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 Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Outcomes

Primary Outcomes

Survival

Time Frame: 1 month

Compare survival in the hospital after admission in Intensive Care Unit in the manner of care

Secondary Outcomes

  • Survival in long-term(10 years)

Investigators

Sponsor
French Cardiology Society
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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