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Pneumological Acute Coronary Syndrom (ACS) Phenotyping Aachen (PAPA)

R

RWTH Aachen University

Status

Completed

Conditions

Acute Coronary Syndrom
Chronic Obstructive Pulmonary Syndrom

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

In this open, monocentric, observational study acute coronary syndrom (ACS) patients will be characterized by pneumological examination concerning a concomitant chronic obstructive pulmonary disease (COPD). Often COPD coexists with ACS; therefore ACS patients benefit either from prevention or potential therapy of chronic hypoxia.

Full description

In this study patients with either non ST-segment-elevation myocardial infarction (NSTEMI) or ST-segment-elevation myocardial infarction (STEMI) will be included. After amnesis patients will undergo blood withdrawal, blood-gas analysis and examinations concerning pulmonary function (Bodyplethysmography). In addition to routine blood withdrawal for differential blood count, 9 ml blood sample is takenfor molecular analysis of relevant prognostic chronic obstructive pulmonary disease (COPD)-blood based biomarkers, an for establishing a library of biomaterial in form of a biobank.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Written declaration of consent
  • Patients with acute myocardial infarct which can be either non ST-segment-elevation myocardial infarct (NSTEMI) or ST-segment-elevation myocardial infarct (STEMI), in both cases exaggeration of cardiac ischaemic markers

Exclusion criteria

  • Patients not fulfilling the incluson criterias or:
  • Pregnant or breastfeeding women
  • Participation in other studies
  • Persons in depency from the sponsor or working with the sponsor
  • Persons without mental ability or capacity to understand and follow the instructions of the investigator

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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