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Eligibility Chronic Kidney Disease NCT00852969

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of ckd stage 2 (gfr >60 and microalbuminuria/proteinuria) and stage 3-4 (gfr 15-30)
Description

Chronic Kidney Disease Stage | Glomerular Filtration Rate | Microalbuminuria | Proteinuria

Data type

boolean

Alias
UMLS CUI [1,1]
C1561643
UMLS CUI [1,2]
C2074731
UMLS CUI [2]
C0017654
UMLS CUI [3]
C0730345
UMLS CUI [4]
C0033687
hdl-cholesterol <50 for men and <55 for women
Description

Serum HDL cholesterol measurement | Gender

Data type

boolean

Alias
UMLS CUI [1]
C0428472
UMLS CUI [2]
C0079399
if taking a statin, stable dose for past one month
Description

Statin Dose Stable

Data type

boolean

Alias
UMLS CUI [1,1]
C0360714
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0205360
glucose <200 mg/dl and hba1c <9%
Description

Glucose measurement | Glucohemoglobin measurement

Data type

boolean

Alias
UMLS CUI [1]
C0337438
UMLS CUI [2]
C0202054
transplant recipients who are in stage 2-3 ckd; 1-year post transplant; and have had no rejection episodes in the 6-months prior to study entry
Description

Transplant Recipients | Chronic Kidney Disease Stage | Transplantation Status post | Rejection episode Absent

Data type

boolean

Alias
UMLS CUI [1]
C0376387
UMLS CUI [2,1]
C1561643
UMLS CUI [2,2]
C2074731
UMLS CUI [3,1]
C0040732
UMLS CUI [3,2]
C0231290
UMLS CUI [4,1]
C0877542
UMLS CUI [4,2]
C0332197
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
hospitalization within prior 3 months
Description

Hospitalization

Data type

boolean

Alias
UMLS CUI [1]
C0019993
any of the following conditions:
Description

Condition Specified Any

Data type

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C0205369
UMLS CUI [1,3]
C1552551
uncontrolled peptic ulcer disease
Description

Peptic Ulcer Uncontrolled

Data type

boolean

Alias
UMLS CUI [1,1]
C0030920
UMLS CUI [1,2]
C0205318
active liver disease or abnormal sgot/sgpt
Description

Liver disease | SGOT abnormal | SGPT abnormal

Data type

boolean

Alias
UMLS CUI [1]
C0023895
UMLS CUI [2]
C0580475
UMLS CUI [3]
C0580469
history of adverse reaction to niacin
Description

Nicotinic acid adverse reaction

Data type

boolean

Alias
UMLS CUI [1]
C0570374
contra-indication to aspirin
Description

Medical contraindication Aspirin

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0004057
concurrent fibrate therapy
Description

Fibrates

Data type

boolean

Alias
UMLS CUI [1]
C1449704
history of gout
Description

Gout

Data type

boolean

Alias
UMLS CUI [1]
C0018099
serum phosphorus levels below 2.7mg/dl
Description

serum phosphorus measurement

Data type

boolean

Alias
UMLS CUI [1]
C2229833
nursing
Description

Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0006147
pregnancy
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
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Similar models

Eligibility Chronic Kidney Disease NCT00852969

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Chronic Kidney Disease Stage | Glomerular Filtration Rate | Microalbuminuria | Proteinuria
Item
diagnosis of ckd stage 2 (gfr >60 and microalbuminuria/proteinuria) and stage 3-4 (gfr 15-30)
boolean
C1561643 (UMLS CUI [1,1])
C2074731 (UMLS CUI [1,2])
C0017654 (UMLS CUI [2])
C0730345 (UMLS CUI [3])
C0033687 (UMLS CUI [4])
Serum HDL cholesterol measurement | Gender
Item
hdl-cholesterol <50 for men and <55 for women
boolean
C0428472 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
Statin Dose Stable
Item
if taking a statin, stable dose for past one month
boolean
C0360714 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
Glucose measurement | Glucohemoglobin measurement
Item
glucose <200 mg/dl and hba1c <9%
boolean
C0337438 (UMLS CUI [1])
C0202054 (UMLS CUI [2])
Transplant Recipients | Chronic Kidney Disease Stage | Transplantation Status post | Rejection episode Absent
Item
transplant recipients who are in stage 2-3 ckd; 1-year post transplant; and have had no rejection episodes in the 6-months prior to study entry
boolean
C0376387 (UMLS CUI [1])
C1561643 (UMLS CUI [2,1])
C2074731 (UMLS CUI [2,2])
C0040732 (UMLS CUI [3,1])
C0231290 (UMLS CUI [3,2])
C0877542 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
Item Group
C0680251 (UMLS CUI)
Hospitalization
Item
hospitalization within prior 3 months
boolean
C0019993 (UMLS CUI [1])
Condition Specified Any
Item
any of the following conditions:
boolean
C0348080 (UMLS CUI [1,1])
C0205369 (UMLS CUI [1,2])
C1552551 (UMLS CUI [1,3])
Peptic Ulcer Uncontrolled
Item
uncontrolled peptic ulcer disease
boolean
C0030920 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
Liver disease | SGOT abnormal | SGPT abnormal
Item
active liver disease or abnormal sgot/sgpt
boolean
C0023895 (UMLS CUI [1])
C0580475 (UMLS CUI [2])
C0580469 (UMLS CUI [3])
Nicotinic acid adverse reaction
Item
history of adverse reaction to niacin
boolean
C0570374 (UMLS CUI [1])
Medical contraindication Aspirin
Item
contra-indication to aspirin
boolean
C1301624 (UMLS CUI [1,1])
C0004057 (UMLS CUI [1,2])
Fibrates
Item
concurrent fibrate therapy
boolean
C1449704 (UMLS CUI [1])
Gout
Item
history of gout
boolean
C0018099 (UMLS CUI [1])
serum phosphorus measurement
Item
serum phosphorus levels below 2.7mg/dl
boolean
C2229833 (UMLS CUI [1])
Breast Feeding
Item
nursing
boolean
C0006147 (UMLS CUI [1])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
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