Eligibility Coronary Artery Disease NCT02410993

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients ≥ 19 years old
Descrizione

ID.1

Tipo di dati

boolean

left main disease, three-vessel disease or two-vessel disease with proximal lad stenosis.
Descrizione

ID.2

Tipo di dati

boolean

Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous pci within 1 year
Descrizione

ID.3

Tipo di dati

boolean

previous sternotomy
Descrizione

ID.4

Tipo di dati

boolean

primary pci for stemi
Descrizione

ID.5

Tipo di dati

boolean

contraindication or hypersensitivity to anti-platelet medications or contrast media
Descrizione

ID.6

Tipo di dati

boolean

planned need for concomitant other cardiac surgery (eg, valve surgery or resection of aortic or left ventricular aneurysm, etc)
Descrizione

ID.7

Tipo di dati

boolean

pregnant women or women with potential childbearing
Descrizione

ID.8

Tipo di dati

boolean

inability to follow the patient over the period of 1 year after enrollment, as assessed by the investigator
Descrizione

ID.9

Tipo di dati

boolean

inability to understand or read the informed content
Descrizione

ID.10

Tipo di dati

boolean

Similar models

Eligibility Coronary Artery Disease NCT02410993

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patients ≥ 19 years old
boolean
ID.2
Item
left main disease, three-vessel disease or two-vessel disease with proximal lad stenosis.
boolean
Item Group
C0680251 (UMLS CUI)
ID.3
Item
previous pci within 1 year
boolean
ID.4
Item
previous sternotomy
boolean
ID.5
Item
primary pci for stemi
boolean
ID.6
Item
contraindication or hypersensitivity to anti-platelet medications or contrast media
boolean
ID.7
Item
planned need for concomitant other cardiac surgery (eg, valve surgery or resection of aortic or left ventricular aneurysm, etc)
boolean
ID.8
Item
pregnant women or women with potential childbearing
boolean
ID.9
Item
inability to follow the patient over the period of 1 year after enrollment, as assessed by the investigator
boolean
ID.10
Item
inability to understand or read the informed content
boolean