ID

40709

Beskrivning

Uric Acid and the Endothelium is CKD; ODM derived from: https://clinicaltrials.gov/show/NCT01228903

Länk

https://clinicaltrials.gov/show/NCT01228903

Nyckelord

  1. 2020-05-01 2020-05-01 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

1 maj 2020

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Kidney Disease NCT01228903

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])

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