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Eligibility Cardiovascular Disease NCT00874432

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age > 60 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
bp 120/80 or higher *(bps will be checked weekly first 4 weeks to ensure < 130/80- if bp remains > 130/80 we will administer other bp meds per jnc vii guidelines)
Description

Blood Pressure

Data type

boolean

Alias
UMLS CUI [1]
C0005823
ckd stage 3 (gfr 30 - 59 ml/min) for ckd group; no ckd for control group
Description

Chronic Kidney Disease stage | Glomerular Filtration Rate

Data type

boolean

Alias
UMLS CUI [1,1]
C1561643
UMLS CUI [1,2]
C2074731
UMLS CUI [2]
C0017654
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
known significant cvd (history of mi, recurrent stroke, or nyha class iii or greater).
Description

Cardiovascular Diseases | Myocardial Infarction | Cerebrovascular accident Recurrent | New York Heart Association Classification

Data type

boolean

Alias
UMLS CUI [1]
C0007222
UMLS CUI [2]
C0027051
UMLS CUI [3,1]
C0038454
UMLS CUI [3,2]
C2945760
UMLS CUI [4]
C1275491
serum potassium > 5.2 meq/l
Description

Serum potassium measurement

Data type

boolean

Alias
UMLS CUI [1]
C0302353
known allergy or hypersensitivity to ace inhibitor or arb
Description

Angiotensin-converting-enzyme inhibitor allergy | Allergy to angiotensin II receptor antagonist

Data type

boolean

Alias
UMLS CUI [1]
C0571939
UMLS CUI [2]
C2585204
female of childbearing age not practicing contraception
Description

Childbearing Potential Contraceptive methods Lacking

Data type

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0700589
UMLS CUI [1,3]
C0332268
current treatment with an ace-i or arb (note: can participate if on ace-i after 6 week washout period)
Description

Angiotensin-Converting Enzyme Inhibitors | Angiotensin II receptor antagonist

Data type

boolean

Alias
UMLS CUI [1]
C0003015
UMLS CUI [2]
C0521942
history of ace-i induced angioedema
Description

Angioedema ACE-I induced

Data type

boolean

Alias
UMLS CUI [1,1]
C0002994
UMLS CUI [1,2]
C0003015
UMLS CUI [1,3]
C0205263
history of angioedema, hereditary or idiopathic
Description

Angioedemas, Hereditary | Idiopathic angioedema

Data type

boolean

Alias
UMLS CUI [1]
C0019243
UMLS CUI [2]
C1304177
persons lacking consent capacity
Description

Informed Consent Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
500 mg/dl proteinuria on 2 consecutive spot urine protein/creat ratios
Description

Proteinuria | Urine protein/creatinine ratio measurement Quantity

Data type

boolean

Alias
UMLS CUI [1]
C0033687
UMLS CUI [2,1]
C1096054
UMLS CUI [2,2]
C1265611
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Similar models

Eligibility Cardiovascular Disease NCT00874432

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age > 60 years
boolean
C0001779 (UMLS CUI [1])
Blood Pressure
Item
bp 120/80 or higher *(bps will be checked weekly first 4 weeks to ensure < 130/80- if bp remains > 130/80 we will administer other bp meds per jnc vii guidelines)
boolean
C0005823 (UMLS CUI [1])
Chronic Kidney Disease stage | Glomerular Filtration Rate
Item
ckd stage 3 (gfr 30 - 59 ml/min) for ckd group; no ckd for control group
boolean
C1561643 (UMLS CUI [1,1])
C2074731 (UMLS CUI [1,2])
C0017654 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Cardiovascular Diseases | Myocardial Infarction | Cerebrovascular accident Recurrent | New York Heart Association Classification
Item
known significant cvd (history of mi, recurrent stroke, or nyha class iii or greater).
boolean
C0007222 (UMLS CUI [1])
C0027051 (UMLS CUI [2])
C0038454 (UMLS CUI [3,1])
C2945760 (UMLS CUI [3,2])
C1275491 (UMLS CUI [4])
Serum potassium measurement
Item
serum potassium > 5.2 meq/l
boolean
C0302353 (UMLS CUI [1])
Angiotensin-converting-enzyme inhibitor allergy | Allergy to angiotensin II receptor antagonist
Item
known allergy or hypersensitivity to ace inhibitor or arb
boolean
C0571939 (UMLS CUI [1])
C2585204 (UMLS CUI [2])
Childbearing Potential Contraceptive methods Lacking
Item
female of childbearing age not practicing contraception
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Angiotensin-Converting Enzyme Inhibitors | Angiotensin II receptor antagonist
Item
current treatment with an ace-i or arb (note: can participate if on ace-i after 6 week washout period)
boolean
C0003015 (UMLS CUI [1])
C0521942 (UMLS CUI [2])
Angioedema ACE-I induced
Item
history of ace-i induced angioedema
boolean
C0002994 (UMLS CUI [1,1])
C0003015 (UMLS CUI [1,2])
C0205263 (UMLS CUI [1,3])
Angioedemas, Hereditary | Idiopathic angioedema
Item
history of angioedema, hereditary or idiopathic
boolean
C0019243 (UMLS CUI [1])
C1304177 (UMLS CUI [2])
Informed Consent Unable
Item
persons lacking consent capacity
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Proteinuria | Urine protein/creatinine ratio measurement Quantity
Item
500 mg/dl proteinuria on 2 consecutive spot urine protein/creat ratios
boolean
C0033687 (UMLS CUI [1])
C1096054 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
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