Eligibility Criteria

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

Inclusion Criteria

Male or female patients
Beschreibung

Male or female patients

Datentyp

boolean

Alias
UMLS CUI-1
C0079399
18 years or more
Beschreibung

18 years or more

Datentyp

boolean

Alias
UMLS CUI-1
C0001779
Presenting with chest pain
Beschreibung

Presenting with chest pain

Datentyp

boolean

Alias
UMLS CUI-1
C0008031
No coronary bypass graft
Beschreibung

No coronary bypass graft

Datentyp

boolean

Alias
UMLS CUI-1
C0010055
No PCI
Beschreibung

No PCI

Datentyp

boolean

Alias
UMLS CUI-1
C1532338
Evidence of a personally signed and dated informed consent document
Beschreibung

Evidence of a personally signed and dated informed consent document

Datentyp

boolean

Alias
UMLS CUI-1
C0021430
Recieved Dalteparin
Beschreibung

Recieved Dalteparin

Datentyp

boolean

Alias
UMLS CUI-1
C0206461
Exclusion Criteria
Beschreibung

Exclusion Criteria

Dalteparin contraindicated
Beschreibung

Dalteparin contraindicated

Datentyp

boolean

Alias
UMLS CUI-1
C0206461
UMLS CUI-2
C0522473

Ähnliche Modelle

Eligibility Criteria

  1. StudyEvent: ODM
    1. Eligibility Criteria
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Inclusion Criteria
Gender
Item
Male or female patients
boolean
C0079399 (UMLS CUI-1)
Age
Item
18 years or more
boolean
C0001779 (UMLS CUI-1)
Chest pain
Item
Presenting with chest pain
boolean
C0008031 (UMLS CUI-1)
CABG
Item
No coronary bypass graft
boolean
C0010055 (UMLS CUI-1)
PCI
Item
No PCI
boolean
C1532338 (UMLS CUI-1)
Informed consent
Item
Evidence of a personally signed and dated informed consent document
boolean
C0021430 (UMLS CUI-1)
Dalteparin
Item
Recieved Dalteparin
boolean
C0206461 (UMLS CUI-1)
Item Group
Exclusion Criteria
Dalteparin contraindicated
Item
Dalteparin contraindicated
boolean
C0206461 (UMLS CUI-1)
C0522473 (UMLS CUI-2)