Engels

Eligibility Coronary Artery Disease NCT00287690

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged 30-75 years
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
patients requiring diagnostic coronary angiography
Beschrijving

Diagnostic coronary angiography

Datatype

boolean

Alias
UMLS CUI [1]
C0085532
presence of coronary artery disease on angiogram but with at least one non-obstructed (lesions <70% narrowed compared with the adjacent normal part of the vessel) atheromatous vessel (confirmed at diagnostic cardiac catheterisation)
Beschrijving

Coronary artery status

Datatype

boolean

Alias
UMLS CUI [1,1]
C1956346
UMLS CUI [1,2]
C0085532
UMLS CUI [2,1]
C0264956
UMLS CUI [2,2]
C0018795
female patients must be postmenopausal (fsh>40 iu/l)
Beschrijving

FSH measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0202022
willing to give informed, written consent
Beschrijving

Informed, written consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
age <30 or >75 years
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
allergy to radiographic contrast media
Beschrijving

Contrast media allergy

Datatype

boolean

Alias
UMLS CUI [1]
C0570562
sino-atrial disease or significant bradycardia
Beschrijving

Sino-atrial disease or bradycardia

Datatype

boolean

Alias
UMLS CUI [1]
C0428908
UMLS CUI [2]
C0428977
concomitant medication with persantin (dipyridamole) or theophyllines
Beschrijving

Persantin or theophyllines

Datatype

boolean

Alias
UMLS CUI [1]
C0012582
UMLS CUI [2]
C0039771
asthma
Beschrijving

Asthma

Datatype

boolean

Alias
UMLS CUI [1]
C0004096
hypertension
Beschrijving

Hypertension

Datatype

boolean

Alias
UMLS CUI [1]
C0020538
left ventricular hypertrophy or dysfunction (clinical/ecg/echo/cxr)
Beschrijving

dysfunction

Datatype

boolean

Alias
UMLS CUI [1]
C0149721
UMLS CUI [2]
C0242698
female patients with fsh<40 iu/l (postmenopausal)
Beschrijving

FSH measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0202022
female patients currently taking hormone therapy, or who have taken hormone therapy in previous 6 months
Beschrijving

Female patients: Hormone therapy

Datatype

boolean

Alias
UMLS CUI [1,1]
C0279025
UMLS CUI [1,2]
C0015780
unwilling to give written informed consent
Beschrijving

Unwilling to written informed consent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0558080
participation in another study within previous 60 days
Beschrijving

Participation status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
Terug naar het begin van de pagina

Similar models

Eligibility Coronary Artery Disease NCT00287690

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
aged 30-75 years
boolean
C0001779 (UMLS CUI [1])
Diagnostic coronary angiography
Item
patients requiring diagnostic coronary angiography
boolean
C0085532 (UMLS CUI [1])
Coronary artery status
Item
presence of coronary artery disease on angiogram but with at least one non-obstructed (lesions <70% narrowed compared with the adjacent normal part of the vessel) atheromatous vessel (confirmed at diagnostic cardiac catheterisation)
boolean
C1956346 (UMLS CUI [1,1])
C0085532 (UMLS CUI [1,2])
C0264956 (UMLS CUI [2,1])
C0018795 (UMLS CUI [2,2])
FSH measurement
Item
female patients must be postmenopausal (fsh>40 iu/l)
boolean
C0202022 (UMLS CUI [1])
Informed, written consent
Item
willing to give informed, written consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Age
Item
age <30 or >75 years
boolean
C0001779 (UMLS CUI [1])
Contrast media allergy
Item
allergy to radiographic contrast media
boolean
C0570562 (UMLS CUI [1])
Sino-atrial disease or bradycardia
Item
sino-atrial disease or significant bradycardia
boolean
C0428908 (UMLS CUI [1])
C0428977 (UMLS CUI [2])
Persantin or theophyllines
Item
concomitant medication with persantin (dipyridamole) or theophyllines
boolean
C0012582 (UMLS CUI [1])
C0039771 (UMLS CUI [2])
Asthma
Item
asthma
boolean
C0004096 (UMLS CUI [1])
Hypertension
Item
hypertension
boolean
C0020538 (UMLS CUI [1])
Left ventricular hypertrophy or dysfunction
Item
left ventricular hypertrophy or dysfunction (clinical/ecg/echo/cxr)
boolean
C0149721 (UMLS CUI [1])
C0242698 (UMLS CUI [2])
FSH measurement
Item
female patients with fsh<40 iu/l (postmenopausal)
boolean
C0202022 (UMLS CUI [1])
Female patients: Hormone therapy
Item
female patients currently taking hormone therapy, or who have taken hormone therapy in previous 6 months
boolean
C0279025 (UMLS CUI [1,1])
C0015780 (UMLS CUI [1,2])
Unwilling to written informed consent
Item
unwilling to give written informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
Participation status
Item
participation in another study within previous 60 days
boolean
C2348568 (UMLS CUI [1])
Terug naar het begin van de pagina