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Acute Coronary Syndome With ST Elevation in Northern Lorraine (StemiLor)

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ClinicalTrials.gov Identifier: NCT03355898
Recruitment Status : Completed
First Posted : November 28, 2017
Last Update Posted : November 30, 2017
Sponsor:
Information provided by (Responsible Party):
Centre Hospitalier Régional Metz-Thionville

Brief Summary:
Lorraine is one of the most affected French region by cardiovascular diseases with a mortality rate for ischemic heart disease higher than the national average in 2010. Due to practice change with the new recommandations of the European Society of Cardiology involving the myocardic revascularization, the investigators wanted to compare the Stemi care in 2005-2006, 2010-2011 and 2015 in the CHR Metz-Thionville.

Condition or disease
Acute Coronary Syndrome

Detailed Description:
This monocentric study evaluate the impact of the new recommandations of the European Society of Cardiology in the acute coronary syndrome with ST elevation (Stemi) care. Data is compiled retrospectively from angiographic report and informatic medical record.

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Study Type : Observational
Actual Enrollment : 340 participants
Observational Model: Other
Time Perspective: Retrospective
Official Title: Acute Coronary Syndrome With ST Elevation in Northern Lorraine: Evolution of Clinicals, Epidemiological and Angiographic Data Since 2005
Actual Study Start Date : March 2016
Actual Primary Completion Date : April 2016
Actual Study Completion Date : June 2016



Primary Outcome Measures :
  1. Acute coronary syndrome with ST elevation care [ Time Frame: Day 1 ]
    Percentage of per-cutaneous angioplasty and percentage of pre-hospital thrombolysis


Secondary Outcome Measures :
  1. Stenting procedure [ Time Frame: Day 1 ]
    Percentage of manual thrombectomy and percentage of direct stenting

  2. Hospital mortality [ Time Frame: Day 1 ]
    Percentage of death during the STEMI care

  3. Epidemiology data [ Time Frame: Day 1 ]
    Mean age of STEMI patients



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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients with an acute coronary syndrome with ST elevation in the CHR Metz-Thionville in 2005-2006, 2010-2011 and 2015
Criteria

Inclusion Criteria:

  • Patient with an acute coronary syndrome with ST elevation for less than 12 hours
  • Patients with coronarography in a context of cardiorespiratory arrest with unknown cause and acute coronary occlusion

Exclusion Criteria:

-

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Responsible Party: Centre Hospitalier Régional Metz-Thionville
ClinicalTrials.gov Identifier: NCT03355898    
Other Study ID Numbers: 2016-06Obs-CHRMT
First Posted: November 28, 2017    Key Record Dates
Last Update Posted: November 30, 2017
Last Verified: November 2017

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Acute Coronary Syndrome
Syndrome
Disease
Pathologic Processes
Myocardial Ischemia
Heart Diseases
Cardiovascular Diseases
Vascular Diseases