Informatie:
Fout:
ID
40709
Beschrijving
Uric Acid and the Endothelium is CKD; ODM derived from: https://clinicaltrials.gov/show/NCT01228903
Link
https://clinicaltrials.gov/show/NCT01228903
Trefwoorden
Versies (1)
- 01-05-20 01-05-20 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
1 mei 2020
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Kidney Disease NCT01228903
Eligibility Kidney Disease NCT01228903
- StudyEvent: Eligibility
Similar models
Eligibility Kidney Disease NCT01228903
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
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])
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])
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])
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])
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])
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])
C0332185 (UMLS CUI [1,2])
Communicable Disease | Antibiotics
Item
active infection, on antibiotics
boolean
C0009450 (UMLS CUI [1])
C0003232 (UMLS CUI [2])
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])
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])
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])
C0002144 (UMLS CUI [1,2])
Therapeutic immunosuppression
Item
immunosuppressive therapy within the last 1 yr
boolean
C0021079 (UMLS CUI [1])