Eligibility Kidney Disease NCT01228903

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
individuals with moderate chronic kidney disease (ckd stage iii) with estimated glomerular filtration rates between 30-60 ml/min/ 1.73m2
Beskrivning

Chronic Kidney Disease Moderate Stage | Estimated Glomerular Filtration Rate

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1561643
UMLS CUI [1,2]
C0205081
UMLS CUI [1,3]
C2074731
UMLS CUI [2]
C3811844
elevated uric acid levels
Beskrivning

Increased uric acid level

Datatyp

boolean

Alias
UMLS CUI [1]
C0041981
age range: more than 18 years old
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
ability to give informed consent
Beskrivning

Informed Consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
albumin > 3.0 g/dl
Beskrivning

Albumin measurement

Datatyp

boolean

Alias
UMLS CUI [1]
C0201838
bmi < 40 kg/m2
Beskrivning

Body mass index

Datatyp

boolean

Alias
UMLS CUI [1]
C1305855
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
life expectancy < 1.0 years
Beskrivning

Life Expectancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0023671
expected to undergo living related kidney transplant in 6 months
Beskrivning

Kidney Transplantation Expected | Living related donor

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0022671
UMLS CUI [1,2]
C1517001
UMLS CUI [2]
C3494891
pregnant, breast feeding, or unwilling to use adequate birth control
Beskrivning

Pregnancy | Breast Feeding | Contraceptive methods Unwilling

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C0700589
UMLS CUI [3,2]
C0558080
history of severe liver disease
Beskrivning

Liver disease Severe

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0023895
UMLS CUI [1,2]
C0205082
history of severe congestive heart failure
Beskrivning

Congestive heart failure Severe

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C0205082
history of hospitalizations within 3 months
Beskrivning

Hospitalization Recent

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0332185
active infection, on antibiotics
Beskrivning

Communicable Disease | Antibiotics

Datatyp

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2]
C0003232
history of warfarin use or other medications that are contraindicated with allopurinol
Beskrivning

Warfarin | Pharmaceutical Preparations Contraindicated Allopurinol

Datatyp

boolean

Alias
UMLS CUI [1]
C0043031
UMLS CUI [2,1]
C0013227
UMLS CUI [2,2]
C1444657
UMLS CUI [2,3]
C0002144
uncontrolled hypertension
Beskrivning

Uncontrolled hypertension

Datatyp

boolean

Alias
UMLS CUI [1]
C1868885
history of acute gout on allopurinol
Beskrivning

Gout | Allopurinol

Datatyp

boolean

Alias
UMLS CUI [1]
C0018099
UMLS CUI [2]
C0002144
history of adverse reaction to allopurinol
Beskrivning

Adverse reaction Allopurinol

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0559546
UMLS CUI [1,2]
C0002144
immunosuppressive therapy within the last 1 yr
Beskrivning

Therapeutic immunosuppression

Datatyp

boolean

Alias
UMLS CUI [1]
C0021079

Similar models

Eligibility Kidney Disease NCT01228903

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Chronic Kidney Disease Moderate Stage | Estimated Glomerular Filtration Rate
Item
individuals with moderate chronic kidney disease (ckd stage iii) with estimated glomerular filtration rates between 30-60 ml/min/ 1.73m2
boolean
C1561643 (UMLS CUI [1,1])
C0205081 (UMLS CUI [1,2])
C2074731 (UMLS CUI [1,3])
C3811844 (UMLS CUI [2])
Increased uric acid level
Item
elevated uric acid levels
boolean
C0041981 (UMLS CUI [1])
Age
Item
age range: more than 18 years old
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
ability to give informed consent
boolean
C0021430 (UMLS CUI [1])
Albumin measurement
Item
albumin > 3.0 g/dl
boolean
C0201838 (UMLS CUI [1])
Body mass index
Item
bmi < 40 kg/m2
boolean
C1305855 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Life Expectancy
Item
life expectancy < 1.0 years
boolean
C0023671 (UMLS CUI [1])
Kidney Transplantation Expected | Living related donor
Item
expected to undergo living related kidney transplant in 6 months
boolean
C0022671 (UMLS CUI [1,1])
C1517001 (UMLS CUI [1,2])
C3494891 (UMLS CUI [2])
Pregnancy | Breast Feeding | Contraceptive methods Unwilling
Item
pregnant, breast feeding, or unwilling to use adequate birth control
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0700589 (UMLS CUI [3,1])
C0558080 (UMLS CUI [3,2])
Liver disease Severe
Item
history of severe liver disease
boolean
C0023895 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Congestive heart failure Severe
Item
history of severe congestive heart failure
boolean
C0018802 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Hospitalization Recent
Item
history of hospitalizations within 3 months
boolean
C0019993 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
Communicable Disease | Antibiotics
Item
active infection, on antibiotics
boolean
C0009450 (UMLS CUI [1])
C0003232 (UMLS CUI [2])
Warfarin | Pharmaceutical Preparations Contraindicated Allopurinol
Item
history of warfarin use or other medications that are contraindicated with allopurinol
boolean
C0043031 (UMLS CUI [1])
C0013227 (UMLS CUI [2,1])
C1444657 (UMLS CUI [2,2])
C0002144 (UMLS CUI [2,3])
Uncontrolled hypertension
Item
uncontrolled hypertension
boolean
C1868885 (UMLS CUI [1])
Gout | Allopurinol
Item
history of acute gout on allopurinol
boolean
C0018099 (UMLS CUI [1])
C0002144 (UMLS CUI [2])
Adverse reaction Allopurinol
Item
history of adverse reaction to allopurinol
boolean
C0559546 (UMLS CUI [1,1])
C0002144 (UMLS CUI [1,2])
Therapeutic immunosuppression
Item
immunosuppressive therapy within the last 1 yr
boolean
C0021079 (UMLS CUI [1])