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Eligibility Coronary Artery Disease (CAD) NCT00308633

1 Formulaires  
Criteria
Description

Criteria

adults older than 21 years.
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
coronary artery disease established by angiography.
Description

coronary artery disease angiography

Type de données

boolean

Alias
UMLS CUI [1,1]
C1956346
UMLS CUI [1,2]
C0085532
at least two months interval since myocardial infarction or coronary artery bypass surgery.
Description

myocardial infarction, coronary artery bypass surgery interval

Type de données

boolean

Alias
UMLS CUI [1,1]
C0027051
UMLS CUI [1,2]
C1272706
UMLS CUI [2,1]
C0010055
UMLS CUI [2,2]
C1272706
at least one month interval since percutaneous coronary intervention or congestive heart failure symptoms.
Description

percutaneous coronary intervention, congestive heart failure symptoms interval

Type de données

boolean

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C1272706
UMLS CUI [2,1]
C0018802
UMLS CUI [2,2]
C1457887
UMLS CUI [2,3]
C1272706
no medical condition that might prohibit safe participation in cardiac rehabilitation.
Description

safe participation in cardiac rehabilitation

Type de données

boolean

Alias
UMLS CUI [1,1]
C0700431
UMLS CUI [1,2]
C0679823
subject understands protocol and provides written, informed consent in addition to willingness to comply with specified follow-up evaluations.
Description

informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
significant structural heart disease (e.g. hypertrophic or dilated cardiomyopathy, valvular heart disease) as determined by echocardiography.
Description

structural heart disease by echocardiography

Type de données

boolean

Alias
UMLS CUI [1,1]
C1290384
UMLS CUI [1,2]
C0013516
angina pectoris that is prolonged in duration (greater than 20 minutes), or does not respond to nitroglycerin (2 tablets) within 2 weeks of referral to the program.
Description

angina pectoris duration and response to nitroglycerin

Type de données

boolean

Alias
UMLS CUI [1,1]
C0002962
UMLS CUI [1,2]
C0449238
UMLS CUI [2,1]
C0002962
UMLS CUI [2,2]
C0017887
subjects physically unable to perform cardiac rehabilitation protocol due to neurologic or orthopedic conditions.
Description

cardiac rehabilitation ability

Type de données

boolean

Alias
UMLS CUI [1,1]
C0700431
UMLS CUI [1,2]
C0085732
women of childbearing age unless recent pregnancy test is negative.
Description

pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
lactating women.
Description

breast feeding

Type de données

boolean

Alias
UMLS CUI [1]
C0006147
implantable cardioverter-defibrillator (icd)
Description

implantable cardioverter defibrillator

Type de données

boolean

Alias
UMLS CUI [1]
C0162589
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Similar models

Eligibility Coronary Artery Disease (CAD) NCT00308633

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
age
Item
adults older than 21 years.
boolean
C0001779 (UMLS CUI [1])
coronary artery disease angiography
Item
coronary artery disease established by angiography.
boolean
C1956346 (UMLS CUI [1,1])
C0085532 (UMLS CUI [1,2])
myocardial infarction, coronary artery bypass surgery interval
Item
at least two months interval since myocardial infarction or coronary artery bypass surgery.
boolean
C0027051 (UMLS CUI [1,1])
C1272706 (UMLS CUI [1,2])
C0010055 (UMLS CUI [2,1])
C1272706 (UMLS CUI [2,2])
percutaneous coronary intervention, congestive heart failure symptoms interval
Item
at least one month interval since percutaneous coronary intervention or congestive heart failure symptoms.
boolean
C1532338 (UMLS CUI [1,1])
C1272706 (UMLS CUI [1,2])
C0018802 (UMLS CUI [2,1])
C1457887 (UMLS CUI [2,2])
C1272706 (UMLS CUI [2,3])
safe participation in cardiac rehabilitation
Item
no medical condition that might prohibit safe participation in cardiac rehabilitation.
boolean
C0700431 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
informed consent
Item
subject understands protocol and provides written, informed consent in addition to willingness to comply with specified follow-up evaluations.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
structural heart disease by echocardiography
Item
significant structural heart disease (e.g. hypertrophic or dilated cardiomyopathy, valvular heart disease) as determined by echocardiography.
boolean
C1290384 (UMLS CUI [1,1])
C0013516 (UMLS CUI [1,2])
angina pectoris duration and response to nitroglycerin
Item
angina pectoris that is prolonged in duration (greater than 20 minutes), or does not respond to nitroglycerin (2 tablets) within 2 weeks of referral to the program.
boolean
C0002962 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0002962 (UMLS CUI [2,1])
C0017887 (UMLS CUI [2,2])
cardiac rehabilitation ability
Item
subjects physically unable to perform cardiac rehabilitation protocol due to neurologic or orthopedic conditions.
boolean
C0700431 (UMLS CUI [1,1])
C0085732 (UMLS CUI [1,2])
pregnancy
Item
women of childbearing age unless recent pregnancy test is negative.
boolean
C0032961 (UMLS CUI [1])
breast feeding
Item
lactating women.
boolean
C0006147 (UMLS CUI [1])
implantable cardioverter defibrillator
Item
implantable cardioverter-defibrillator (icd)
boolean
C0162589 (UMLS CUI [1])
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