ID

34214

Description

EArly Discharge After Transradial Stenting of CoronarY Arteries in High-Risk Patients of Bleeding; ODM derived from: https://clinicaltrials.gov/show/NCT01084993

Link

https://clinicaltrials.gov/show/NCT01084993

Keywords

  1. 1/15/19 1/15/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 15, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT01084993

Eligibility Coronary Artery Disease NCT01084993

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
at least two of the following additional criteria
Description

ID.1

Data type

boolean

at least 70 yrs old
Description

ID.2

Data type

boolean

female gender
Description

ID.3

Data type

boolean

diabetes
Description

ID.4

Data type

boolean

creatinine clearance <60ml/min
Description

ID.5

Data type

boolean

history of gastro-intestinal or other organ bleeding
Description

ID.6

Data type

boolean

baseline anemia
Description

ID.7

Data type

boolean

current treatment with glycoproteins iib-iiia inhibitors
Description

ID.8

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
intolerance or allergy to asa, clopidogrel or ticlopidine precluding treatment for 12 months
Description

ID.9

Data type

boolean

concurrent participation in other investigational study
Description

ID.10

Data type

boolean

femoral sheath (artery)
Description

ID.11

Data type

boolean

Similar models

Eligibility Coronary Artery Disease NCT01084993

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
at least two of the following additional criteria
boolean
ID.2
Item
at least 70 yrs old
boolean
ID.3
Item
female gender
boolean
ID.4
Item
diabetes
boolean
ID.5
Item
creatinine clearance <60ml/min
boolean
ID.6
Item
history of gastro-intestinal or other organ bleeding
boolean
ID.7
Item
baseline anemia
boolean
ID.8
Item
current treatment with glycoproteins iib-iiia inhibitors
boolean
Item Group
C0680251 (UMLS CUI)
ID.9
Item
intolerance or allergy to asa, clopidogrel or ticlopidine precluding treatment for 12 months
boolean
ID.10
Item
concurrent participation in other investigational study
boolean
ID.11
Item
femoral sheath (artery)
boolean

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