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Eligibility Coronary Artery Disease NCT02093845

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Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
all patients aged ≥18 years who are eligible for treatment with one or several drug-eluting coronary stents at one of the three heart centers in odense, skejby and aalborg can be included in the study.
Beschrijving

Age | Patients Eligible Drug-Eluting Coronary Stents

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2,1]
C0030705
UMLS CUI [2,2]
C1548635
UMLS CUI [2,3]
C1262327
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
age < 18 years
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
the patient does not wish to participate
Beschrijving

Study Subject Participation Status Unwilling

Datatype

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0558080
the patient is not able to consent to randomization (eg intubated patients)
Beschrijving

Randomization Consent Unable | Patients Intubation

Datatype

boolean

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C1511481
UMLS CUI [1,3]
C1299582
UMLS CUI [2,1]
C0030705
UMLS CUI [2,2]
C0021925
the patient do not live in west denmark
Beschrijving

Patient Foreign National

Datatype

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0870575
the patient do not speak danish
Beschrijving

Lacking Able to speak Danish language

Datatype

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C0564215
UMLS CUI [1,3]
C0010969
the patient is already included in this study
Beschrijving

Study Subject Participation Status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
the patient is already participating in other stent studies
Beschrijving

Study Subject Participation Status | Stent Clinical Trial

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0038257
UMLS CUI [2,2]
C0008976
life expectancy <1 year
Beschrijving

Life Expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
allergic to aspirin, clopidogrel, prasugrel or ticagrelor
Beschrijving

Aspirin allergy | Hypersensitivity Clopidogrel | Hypersensitivity Prasugrel | Hypersensitivity Ticagrelor

Datatype

boolean

Alias
UMLS CUI [1]
C0004058
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0070166
UMLS CUI [3,1]
C0020517
UMLS CUI [3,2]
C1620287
UMLS CUI [4,1]
C0020517
UMLS CUI [4,2]
C1999375
allergic to everolimus or biolimus
Beschrijving

Hypersensitivity Everolimus | Hypersensitivity Biolimus A9

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0541315
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C4310325
only implanted bms
Beschrijving

Bare metal stent implanted only

Datatype

boolean

Alias
UMLS CUI [1,1]
C2825200
UMLS CUI [1,2]
C0021102
UMLS CUI [1,3]
C0205171
only performed poba
Beschrijving

Other Coding

Datatype

boolean

Alias
UMLS CUI [1]
C3846158
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Similar models

Eligibility Coronary Artery Disease NCT02093845

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age | Patients Eligible Drug-Eluting Coronary Stents
Item
all patients aged ≥18 years who are eligible for treatment with one or several drug-eluting coronary stents at one of the three heart centers in odense, skejby and aalborg can be included in the study.
boolean
C0001779 (UMLS CUI [1])
C0030705 (UMLS CUI [2,1])
C1548635 (UMLS CUI [2,2])
C1262327 (UMLS CUI [2,3])
Item Group
C0680251 (UMLS CUI)
Age
Item
age < 18 years
boolean
C0001779 (UMLS CUI [1])
Study Subject Participation Status Unwilling
Item
the patient does not wish to participate
boolean
C2348568 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
Randomization Consent Unable | Patients Intubation
Item
the patient is not able to consent to randomization (eg intubated patients)
boolean
C0034656 (UMLS CUI [1,1])
C1511481 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C0030705 (UMLS CUI [2,1])
C0021925 (UMLS CUI [2,2])
Patient Foreign National
Item
the patient do not live in west denmark
boolean
C0030705 (UMLS CUI [1,1])
C0870575 (UMLS CUI [1,2])
Lacking Able to speak Danish language
Item
the patient do not speak danish
boolean
C0332268 (UMLS CUI [1,1])
C0564215 (UMLS CUI [1,2])
C0010969 (UMLS CUI [1,3])
Study Subject Participation Status
Item
the patient is already included in this study
boolean
C2348568 (UMLS CUI [1])
Study Subject Participation Status | Stent Clinical Trial
Item
the patient is already participating in other stent studies
boolean
C2348568 (UMLS CUI [1])
C0038257 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
Life Expectancy
Item
life expectancy <1 year
boolean
C0023671 (UMLS CUI [1])
Aspirin allergy | Hypersensitivity Clopidogrel | Hypersensitivity Prasugrel | Hypersensitivity Ticagrelor
Item
allergic to aspirin, clopidogrel, prasugrel or ticagrelor
boolean
C0004058 (UMLS CUI [1])
C0020517 (UMLS CUI [2,1])
C0070166 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C1620287 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C1999375 (UMLS CUI [4,2])
Hypersensitivity Everolimus | Hypersensitivity Biolimus A9
Item
allergic to everolimus or biolimus
boolean
C0020517 (UMLS CUI [1,1])
C0541315 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C4310325 (UMLS CUI [2,2])
Bare metal stent implanted only
Item
only implanted bms
boolean
C2825200 (UMLS CUI [1,1])
C0021102 (UMLS CUI [1,2])
C0205171 (UMLS CUI [1,3])
Other Coding
Item
only performed poba
boolean
C3846158 (UMLS CUI [1])
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