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Stent For Life Observatory (SFL)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01251198
First Posted: December 1, 2010
Last Update Posted: June 14, 2012
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Martine Gilard, French Cardiology Society
  Purpose
Observatory multicenter, prospective, to support the acute phase of acute coronary syndromes with ST segment elevation ST (myocardial infarction).

Condition
Acute Coronary Syndrome Myocardial Infarction

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Stent For Life Observatory

Resource links provided by NLM:


Further study details as provided by Martine Gilard, French Cardiology Society:

Enrollment: 460
Study Start Date: November 2010
Study Completion Date: March 2012
Primary Completion Date: February 2012 (Final data collection date for primary outcome measure)
Groups/Cohorts
Acute coronary Syndrome
Patients affected are patients with acute coronary syndrome with ST segment elevation ST (myocardial infarction) in 48 hospitalized in one of the centers (emergency, ambulance, intensive care unit, cardiac catheterization lab).

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients affected are patients with acute coronary syndrome with ST segment elevation ST (myocardial infarction) in 48 hospitalized in one of the centers (emergency, ambulance, intensive care unit, cardiac catheterization lab).
Criteria

Inclusion Criteria:

  • Any patient with a myocardial infarction less than 48 hours during the November 2010 is eligible and should be considered for inclusion in the study.
  • Every patient who agreed to participate in the study

Exclusion Criteria:

  • Patients with myocardial infarction after a coronary revascularization, or after cardiac surgery or extra heartbeat.
  • Patient denying that his personal data are subject to treatment automated
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01251198


Locations
France
CHU Brest
Brest, France
Sponsors and Collaborators
French Cardiology Society
Investigators
Principal Investigator: Martine Gilard Assistance Publique - Hôpitaux de Paris
  More Information

Publications:
Responsible Party: Martine Gilard, Professor, French Cardiology Society
ClinicalTrials.gov Identifier: NCT01251198     History of Changes
Other Study ID Numbers: Stent For Life
First Submitted: November 30, 2010
First Posted: December 1, 2010
Last Update Posted: June 14, 2012
Last Verified: June 2012

Additional relevant MeSH terms:
Infarction
Myocardial Infarction
Acute Coronary Syndrome
Ischemia
Pathologic Processes
Necrosis
Myocardial Ischemia
Heart Diseases
Cardiovascular Diseases
Vascular Diseases