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NCT Number: NCT02355457

Biomarkers in Acute Cardiac Care

The primary aim of the study is to investigate new cardiac biomarkers and algorithms to diagnose acute coronary syndrome in patients with suspected acute myocardial infarction.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Cardiology, University Heart Center Hamburg

Hamburg, 20246, Germany

Location status: Recruiting

Location contact

Johannes Neumann, MD

CONTACT

[email protected]

0049407410 ext. 56800

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Symptoms suggestive of acute myocardial infarction
  • Ability to provide written informed consent in accordance with Good epidemiological Practice and local legislation
  • Individuals at least 18 years old

Exclusion criteria

  • Insufficient knowledge of the German language (able to understand and write the German language)

Treatment and study plan

Primary outcomes

  1. Acute myocardial infarction as index event

    Time frame: Months

    The primary endpoint of the study is acute myocardial infarction

Secondary outcomes

  1. AMI, Mortality, heart failure and quality of life

    Time frame: Years

    The secondary endpoint of the study is mortality, heart failure, quality of life.

Study contacts

Contact information is provided by the study sponsor or research team.

Johannes T Neumann, MD

CONTACT

[email protected]

0049407410 ext. 56800

Nils Sörensen, MD

CONTACT

[email protected]

0049407410 ext. 56800

Sponsors and collaborators

Lead sponsor

Universitätsklinikum Hamburg-Eppendorf

Other

Registry information

Acronym: BACC

Important dates

Study start
2013
Primary completion
2027
Study completion
2027
First posted
Feb 4, 2015
Registry last updated
May 13, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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