ID

11731

Descripción

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.

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Versiones (1)
  1. 28/7/15 28/7/15 -
Subido en

28 de julio de 2015

DOI

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Licencia

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

Inglés

Eligibility criteria

1 formularios  
  1. StudyEvent: ODM
    1. Eligibility criteria
Inclusion Criteria
Descripción

Inclusion Criteria

adults > 18 years
Descripción

adults > 18 years

Tipo de datos

boolean

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

able to give informed consent

Tipo de datos

boolean

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

a history of chest pain

Tipo de datos

boolean

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

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

Tipo de datos

boolean

Alias
UMLS CUI-1
C0948089
Exclusion Criteria
Descripción

Exclusion Criteria

< 18 years of age
Descripción

< 18 years of age

Tipo de datos

boolean

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

Unwillingness or incapacity to provide informed consent

Tipo de datos

boolean

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

Prior admission resulting in inclusion in the present study

Tipo de datos

boolean

Alias
UMLS CUI-1
C0422740
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Similar models

Eligibility criteria

1 formularios
  1. StudyEvent: ODM
    1. Eligibility criteria
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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)
Volver a la parte superior de la página 

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