ID

11731

Beschrijving

The main aim of this trial is to assess the long-term prognostic value of different types of Factor XIIa in an unselected, single center series of 871 chest pain patients admitted to the emergency unit, employing blood samples collected at admission. The second purpose of this study is to assess the incremental prognostic value of B-type natriuretic peptide (BNP) and high-sensitive C-reactive protein (hsCRP). A third purpose of this study is to evaluate the prognostic impact of the Omega-3 Index which is a measure of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) relative to other fatty acids in the erythrocyte membrane.

Trefwoorden

Versies (1)
  1. 28-07-15 28-07-15 -
Geüploaded op

28 juli 2015

DOI

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Licentie

Creative Commons BY-NC 3.0
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Eligibility RACS Acute Coronary Syndrome NCT00521976

Engels

Eligibility criteria

1 Formulieren  
  1. StudyEvent: ODM
    1. Eligibility criteria
Inclusion Criteria
Beschrijving

Inclusion Criteria

adults > 18 years
Beschrijving

adults > 18 years

Datatype

boolean

Alias
UMLS CUI-1
C0001779
able to give informed consent
Beschrijving

able to give informed consent

Datatype

boolean

Alias
UMLS CUI-1
C0021430
a history of chest pain
Beschrijving

a history of chest pain

Datatype

boolean

Alias
UMLS CUI-1
C0008031
other symptoms suggestive of an ACS leading to admission at the emergency unit
Beschrijving

other symptoms suggestive of an ACS leading to admission at the emergency unit

Datatype

boolean

Alias
UMLS CUI-1
C0948089
Exclusion Criteria
Beschrijving

Exclusion Criteria

< 18 years of age
Beschrijving

< 18 years of age

Datatype

boolean

Alias
UMLS CUI-1
C0001779
Unwillingness or incapacity to provide informed consent
Beschrijving

Unwillingness or incapacity to provide informed consent

Datatype

boolean

Alias
UMLS CUI-1
C0021430
Prior admission resulting in inclusion in the present study
Beschrijving

Prior admission resulting in inclusion in the present study

Datatype

boolean

Alias
UMLS CUI-1
C0422740
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Similar models

Eligibility criteria

1 Formulieren
  1. StudyEvent: ODM
    1. Eligibility criteria
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Inclusion Criteria
Age
Item
adults > 18 years
boolean
C0001779 (UMLS CUI-1)
Informed consent
Item
able to give informed consent
boolean
C0021430 (UMLS CUI-1)
Chest pain
Item
a history of chest pain
boolean
C0008031 (UMLS CUI-1)
Acute coronary syndrome
Item
other symptoms suggestive of an ACS leading to admission at the emergency unit
boolean
C0948089 (UMLS CUI-1)
Item Group
Exclusion Criteria
Age
Item
< 18 years of age
boolean
C0001779 (UMLS CUI-1)
Informed consent
Item
Unwillingness or incapacity to provide informed consent
boolean
C0021430 (UMLS CUI-1)
Study patient
Item
Prior admission resulting in inclusion in the present study
boolean
C0422740 (UMLS CUI-1)
Terug naar het begin van de pagina 

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