Eligibility Proteinuria NCT01831193

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of proteinuric chronic kidney disease with 1g or more of proteins in a daily recollection.
Description

Chronic Kidney Disease proteinuric | Urine total protein measurement

Data type

boolean

Alias
UMLS CUI [1,1]
C1561643
UMLS CUI [1,2]
C0850605
UMLS CUI [2]
C0428541
individuals taking angiotensin ii receptor blocker or ace inhibitors in monotherapy with maximum dose or in combination.
Description

Angiotensin II receptor antagonist Dose Maximum | Angiotensin-Converting Enzyme Inhibitors Dose Maximum | Combined Modality Therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C0521942
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0806909
UMLS CUI [2,1]
C0003015
UMLS CUI [2,2]
C0178602
UMLS CUI [2,3]
C0806909
UMLS CUI [3]
C0009429
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
hepatic damage.
Description

Liver damage

Data type

boolean

Alias
UMLS CUI [1]
C0151763
malignancy.
Description

Malignant Neoplasms

Data type

boolean

Alias
UMLS CUI [1]
C0006826
pregnancy.
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
peritoneal or hemodialysis.
Description

Peritoneal Dialysis | Hemodialysis

Data type

boolean

Alias
UMLS CUI [1]
C0031139
UMLS CUI [2]
C0019004
organ transplantation.
Description

Organ Transplantation

Data type

boolean

Alias
UMLS CUI [1]
C0029216
heart failure classification iii or iv (new york heart association).
Description

Heart failure New York Heart Association Classification

Data type

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
history of chemotherapy within 2 years prior to screening.
Description

Chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0392920

Similar models

Eligibility Proteinuria NCT01831193

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Chronic Kidney Disease proteinuric | Urine total protein measurement
Item
diagnosis of proteinuric chronic kidney disease with 1g or more of proteins in a daily recollection.
boolean
C1561643 (UMLS CUI [1,1])
C0850605 (UMLS CUI [1,2])
C0428541 (UMLS CUI [2])
Angiotensin II receptor antagonist Dose Maximum | Angiotensin-Converting Enzyme Inhibitors Dose Maximum | Combined Modality Therapy
Item
individuals taking angiotensin ii receptor blocker or ace inhibitors in monotherapy with maximum dose or in combination.
boolean
C0521942 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0003015 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0806909 (UMLS CUI [2,3])
C0009429 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
Liver damage
Item
hepatic damage.
boolean
C0151763 (UMLS CUI [1])
Malignant Neoplasms
Item
malignancy.
boolean
C0006826 (UMLS CUI [1])
Pregnancy
Item
pregnancy.
boolean
C0032961 (UMLS CUI [1])
Peritoneal Dialysis | Hemodialysis
Item
peritoneal or hemodialysis.
boolean
C0031139 (UMLS CUI [1])
C0019004 (UMLS CUI [2])
Organ Transplantation
Item
organ transplantation.
boolean
C0029216 (UMLS CUI [1])
Heart failure New York Heart Association Classification
Item
heart failure classification iii or iv (new york heart association).
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Chemotherapy
Item
history of chemotherapy within 2 years prior to screening.
boolean
C0392920 (UMLS CUI [1])