- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02961985
Myocardial Infarction Register of the Saarland (MIR-SL)
Myokardinfarkt-Register Des Saarlandes (MIR-SL)
Study Overview
Status
Conditions
Detailed Description
The Myocardial Infarction Register Saarland (MIR-SL), is intended to collect data about the treatment of patients suffering from ST-elevation myocardial infarction (STEMI). It aims to provide current data on the implementation of guidelines for both, the interventional and adjuvant drug therapy of STEMI in daily clinical practice in the Saarland.
In order to obtain representative data for the Saarland, preferably all consecutive patients should be documented comprehensively in the University Hospital of the Saarland, the non-university hospitals with cardiac catheterization laboratory as well as in hospitals without cardiac catheterization laboratory .
MIR-SL is attended by all 22 hospitals in Saarland, that treat patients with acute STEMI. A follow-up will be carried out after three months, 12 months and five years.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Dillingen, Germany
- Marienhaus Klinikum Saarlouis-Dillingen
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Homburg, Germany
- Universitaetsklinikum des Saarlandes
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Saarland
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Saarbruecken, Saarland, Germany, 66119
- Klinikum Saarbruecken
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- signed informed consent
Exclusion Criteria:
- age < 18 years
- missing informed consent
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Rate of reperfusion therapies
Time Frame: 24 hours
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Describe hospital daily routine in Germany
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24 hours
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Time before reperfusion therapy
Time Frame: 24 hours
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pre-hospital time, intrahospital time, transfer time
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24 hours
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In-hospital mortality
Time Frame: 24 hours
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Describe mortality before discharge
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24 hours
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MIR-SL
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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