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NCT02961985 Clinical Trial

Myocardial Infarction Register of the Saarland

Myocardial Infarction Clinical Trial

— MIR-SL  

Official title:
Myokardinfarkt-Register Des Saarlandes (MIR-SL)

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02961985
Other study ID # MIR-SL
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 2016
Est. completion date March 29, 2023

Study information
Verified date April 2023
Source Stiftung Institut fuer Herzinfarktforschung
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial 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.

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.

Recruitment information / eligibility
Status Completed
Enrollment 455
Est. completion date March 29, 2023
Est. primary completion date July 19, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - signed informed consent Exclusion Criteria: - age < 18 years - missing informed consent

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Germany Marienhaus Klinikum Saarlouis-Dillingen Dillingen
Germany Universitaetsklinikum des Saarlandes Homburg
Germany Klinikum Saarbruecken Saarbruecken Saarland

Sponsors (2)
Lead Sponsor Collaborator
Stiftung Institut fuer Herzinfarktforschung Ministry of Social Affairs, Health, Women and Family of Saarland

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary Rate of reperfusion therapies Describe hospital daily routine in Germany 24 hours
Secondary Time before reperfusion therapy pre-hospital time, intrahospital time, transfer time 24 hours
Secondary In-hospital mortality Describe mortality before discharge 24 hours
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