Elegibility Criteria

  1. StudyEvent: ODM
    1. Elegibility Criteria
Inclusion Criteria
Descrizione

Inclusion Criteria

Currently receiving aspirin
Descrizione

Currently receiving aspirin

Tipo di dati

boolean

Alias
UMLS CUI-1
C0004057
Hospitalized with symptoms suggestive of acute coronary syndrome
Descrizione

Hospitalized with symptoms suggestive of acute coronary syndrome

Tipo di dati

boolean

Alias
UMLS CUI-1
C0948089
Exclusion criteria
Descrizione

Exclusion criteria

Significant renal impairment
Descrizione

Significant renal impairment

Tipo di dati

boolean

Alias
UMLS CUI-1
C0035078
Significant liver disease
Descrizione

Significant liver disease

Tipo di dati

boolean

Alias
UMLS CUI-1
C0085605
Need for continued anticoagulant therapy
Descrizione

Need for continued anticoagulant therapy

Tipo di dati

boolean

Alias
UMLS CUI-1
C0150457
Any condition that, in the opinion of the investigator, contraindicates anticoagulant therapy
Descrizione

Any condition that, in the opinion of the investigator, contraindicates anticoagulant therapy

Tipo di dati

boolean

Alias
UMLS CUI-1
C1531588

Similar models

Elegibility Criteria

  1. StudyEvent: ODM
    1. Elegibility Criteria
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Inclusion Criteria
Aspirin
Item
Currently receiving aspirin
boolean
C0004057 (UMLS CUI-1)
Acute coronary syndrome
Item
Hospitalized with symptoms suggestive of acute coronary syndrome
boolean
C0948089 (UMLS CUI-1)
Item Group
Exclusion criteria
Kidney failure
Item
Significant renal impairment
boolean
C0035078 (UMLS CUI-1)
Liver failure
Item
Significant liver disease
boolean
C0085605 (UMLS CUI-1)
Anticoagulant therapy
Item
Need for continued anticoagulant therapy
boolean
C0150457 (UMLS CUI-1)
Anticoagulant contraindicated
Item
Any condition that, in the opinion of the investigator, contraindicates anticoagulant therapy
boolean
C1531588 (UMLS CUI-1)