Eligibility Criteria

  1. StudyEvent: ODM
    1. Eligibility Criteria
Inclusion Criteria
Descrição

Inclusion Criteria

Male or Female
Descrição

Male or Female

Tipo de dados

boolean

Alias
UMLS CUI-1
C0079399
Age > 18
Descrição

Age > 18

Tipo de dados

boolean

Alias
UMLS CUI-1
C0001779
hospitalised for chest pain
Descrição

hospitalised for chest pain

Tipo de dados

boolean

Alias
UMLS CUI-1
C0008031
Potential ACS
Descrição

Potential ACS

Tipo de dados

boolean

Alias
UMLS CUI-1
C0948089
Exclusion Criteria
Descrição

Exclusion Criteria

moderate or severe liver disease
Descrição

moderate or severe liver disease

Tipo de dados

boolean

Alias
UMLS CUI-1
C0085605
treated with blood clotting agents that cannot be stopped
Descrição

treated with blood clotting agents that cannot be stopped

Tipo de dados

boolean

Alias
UMLS CUI-1
C0280087
already been treated with an invasive (angioplasty) procedure
Descrição

already been treated with an invasive (angioplasty) procedure

Tipo de dados

boolean

Alias
UMLS CUI-1
C0190211

Similar models

Eligibility Criteria

  1. StudyEvent: ODM
    1. Eligibility Criteria
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Inclusion Criteria
Gender
Item
Male or Female
boolean
C0079399 (UMLS CUI-1)
Age
Item
Age > 18
boolean
C0001779 (UMLS CUI-1)
Chest Pain
Item
hospitalised for chest pain
boolean
C0008031 (UMLS CUI-1)
Acute coronary syndrome
Item
Potential ACS
boolean
C0948089 (UMLS CUI-1)
Item Group
Exclusion Criteria
Liver failure
Item
moderate or severe liver disease
boolean
C0085605 (UMLS CUI-1)
blood clotting agents
Item
treated with blood clotting agents that cannot be stopped
boolean
C0280087 (UMLS CUI-1)
Coronary angioplasty
Item
already been treated with an invasive (angioplasty) procedure
boolean
C0190211 (UMLS CUI-1)