Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Acute Coronary Syndrome
  • Chest Pain
  • Myocardial Infarction
Design
Observational Model: CohortTime Perspective: Prospective

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

The primary aim of the study is to detect and evaluate new cardiac biomarkers, evaluate and improve acute coronary syndrome (ACS) risk scores, which takes into account clinical, gender specific, psycho-social and lifestyle-risk factors, protein patterns and genetic variability in addition to the cla...

The primary aim of the study is to detect and evaluate new cardiac biomarkers, evaluate and improve acute coronary syndrome (ACS) risk scores, which takes into account clinical, gender specific, psycho-social and lifestyle-risk factors, protein patterns and genetic variability in addition to the classical risk factors with respect to the primary endpoint of acute myocardial infarction. Secondary study aims are : To provide estimates for the incidence of ACS in patients presenting with recent onset chest pain; To provide accurate, quantifiable measures of precursors of ACS; DNA, RNA, cells, and serum/plasma for comprehensive genetic, gene expression and proteomic studies To explore the impact of ACS candidate genes on cardiovascular risk stratification by using genome-wide analyses and a biological systems approach; To explore proteins relevant for ACS; To allow the identification of new therapeutic targets; To evaluate the impact of socio-economic factors on ACS and CAD risk. Patients will be followed up during the hospital stay. Afterwards a telephone follow-up will take place after 30 days, 6, 24 and 48 months.

Tracking Information

NCT #
NCT02355457
Collaborators
Not Provided
Investigators
Principal Investigator: Dirk Westermann, MD UHZ Principal Investigator: Stefan Blankenberg, MD UHZ