Myocardial Infarction Register of the Saarland
MIR-SL
Myokardinfarkt-Register Des Saarlandes (MIR-SL)
1 other identifier
observational
455
1 country
3
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2016
Longer than P75 for all trials
3 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 5, 2016
CompletedStudy Start
First participant enrolled
October 1, 2016
CompletedFirst Posted
Study publicly available on registry
November 11, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 19, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
March 29, 2023
CompletedApril 14, 2023
April 1, 2023
1.8 years
September 5, 2016
April 11, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Rate of reperfusion therapies
Describe hospital daily routine in Germany
24 hours
Secondary Outcomes (2)
Time before reperfusion therapy
24 hours
In-hospital mortality
24 hours
Eligibility Criteria
Patients admitted to a hospital in the Saarland region with ST elevation myocardial infarction, in the last 24 hours.
You may qualify if:
- signed informed consent
You may not qualify if:
- age \< 18 years
- missing informed consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (3)
Klinikum Saarbruecken
Saarbrücken, Saarland, 66119, Germany
Marienhaus Klinikum Saarlouis-Dillingen
Dillingen, Germany
Universitaetsklinikum des Saarlandes
Homburg, Germany
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Anselm K. Gitt, Dr.
Stiftung Institut fuer Herzinfarktforschung
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 5 Years
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 5, 2016
First Posted
November 11, 2016
Study Start
October 1, 2016
Primary Completion
July 19, 2018
Study Completion
March 29, 2023
Last Updated
April 14, 2023
Record last verified: 2023-04
Data Sharing
- IPD Sharing
- Will not share