ID

34223

Descripción

BIOFLOW-III Romania Satellite Registry; ODM derived from: https://clinicaltrials.gov/show/NCT01593059

Link

https://clinicaltrials.gov/show/NCT01593059

Palabras clave

  1. 15/1/19 15/1/19 -
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

15 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT01593059

Eligibility Coronary Artery Disease NCT01593059

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
symptomatic coronary artery disease
Descripción

ID.1

Tipo de datos

boolean

subject has signed informed consent for data release
Descripción

ID.2

Tipo de datos

boolean

subject is geographically stable and willing to participate at all follow-up assessments
Descripción

ID.3

Tipo de datos

boolean

subject is ≥ 18 years
Descripción

ID.4

Tipo de datos

boolean

elective pci with des
Descripción

ID.5

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
subject did not sign informed consent for data release
Descripción

ID.6

Tipo de datos

boolean

pregnancy
Descripción

ID.7

Tipo de datos

boolean

known intolerance to aspirin, clopidogrel, ticlopidine, heparin or any other anticoagulation / antiplatelet therapy required for pci, stainless steel, sirolimus or contrast media
Descripción

ID.8

Tipo de datos

boolean

planned surgery within 6 months of pci unless dual antiplatelet therapy will be maintained
Descripción

ID.9

Tipo de datos

boolean

currently participating in another study and primary endpoint is not reached yet.
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Coronary Artery Disease NCT01593059

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
symptomatic coronary artery disease
boolean
ID.2
Item
subject has signed informed consent for data release
boolean
ID.3
Item
subject is geographically stable and willing to participate at all follow-up assessments
boolean
ID.4
Item
subject is ≥ 18 years
boolean
ID.5
Item
elective pci with des
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
subject did not sign informed consent for data release
boolean
ID.7
Item
pregnancy
boolean
ID.8
Item
known intolerance to aspirin, clopidogrel, ticlopidine, heparin or any other anticoagulation / antiplatelet therapy required for pci, stainless steel, sirolimus or contrast media
boolean
ID.9
Item
planned surgery within 6 months of pci unless dual antiplatelet therapy will be maintained
boolean
ID.10
Item
currently participating in another study and primary endpoint is not reached yet.
boolean

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