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Completed

NCT Number: NCT01237418

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

European Hospital Georges Pompidou

Paris, France

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Survival

    Time frame: 1 month

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

Secondary outcomes

  1. Survival in long-term

    Time frame: 10 years

Sponsors and collaborators

Lead sponsor

French Cardiology Society

Other

Registry information

Acronym: FAST-MI 2010

Important dates

Study start
2010
Primary completion
2020
Study completion
2020
First posted
Nov 9, 2010
Registry last updated
Feb 10, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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