Eligibility criteria

  1. StudyEvent: ODM
    1. Eligibility criteria
Inclusion Criteria
Beskrivning

Inclusion Criteria

Provision of signed informed consent
Beskrivning

Provision of signed informed consent

Datatyp

boolean

Alias
UMLS CUI-1
C0021430
Index event of ST segment elevation ACS
Beskrivning

Index event of non-ST or ST segment elevation ACS

Datatyp

boolean

Alias
UMLS CUI-1
C1536220
Index event of non-ST segment elevation ACS
Beskrivning

Index event of non-ST segment elevation ACS

Datatyp

boolean

Alias
UMLS CUI-1
C3537184
Exclusion criteria
Beskrivning

Exclusion criteria

Index event is an acute complication of percutaneous coronary intervention
Beskrivning

Index event is an acute complication of percutaneous coronary intervention

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C1532338
Patient has undergone Percutaneous Coronary Intervention (PCI) after the index event before the first dose of study treatment
Beskrivning

Patient has undergone Percutaneous Coronary Intervention (PCI) after the index event before the first dose of study treatment

Datatyp

boolean

Alias
UMLS CUI-1
C1532338
Oral anticoagulation therapy that cannot be stopped
Beskrivning

Oral anticoagulation therapy that cannot be stopped

Datatyp

boolean

Alias
UMLS CUI-1
C0003281
The conditions associated with increased risk of bradycardiac events
Beskrivning

The conditions associated with increased risk of bradycardiac events

Datatyp

boolean

Alias
UMLS CUI-1
C0428977

Similar models

Eligibility criteria

  1. StudyEvent: ODM
    1. Eligibility criteria
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Inclusion Criteria
Informed consent
Item
Provision of signed informed consent
boolean
C0021430 (UMLS CUI-1)
STEMI
Item
Index event of ST segment elevation ACS
boolean
C1536220 (UMLS CUI-1)
NSTEMI
Item
Index event of non-ST segment elevation ACS
boolean
C3537184 (UMLS CUI-1)
Item Group
Exclusion criteria
PCI complication
Item
Index event is an acute complication of percutaneous coronary intervention
boolean
C0009566 (UMLS CUI [1,1])
C1532338 (UMLS CUI [1,2])
PCI
Item
Patient has undergone Percutaneous Coronary Intervention (PCI) after the index event before the first dose of study treatment
boolean
C1532338 (UMLS CUI-1)
anticoagulation therapy
Item
Oral anticoagulation therapy that cannot be stopped
boolean
C0003281 (UMLS CUI-1)
Bradycardia
Item
The conditions associated with increased risk of bradycardiac events
boolean
C0428977 (UMLS CUI-1)