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Clinical Trial 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.


Clinical Trial 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


Related Conditions & MeSH terms


NCT number NCT01237418
Study type Observational
Source French Cardiology Society
Contact
Status Active, not recruiting
Phase
Start date October 2010
Completion date December 2022

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