Eligibility Chronic Kidney Disease NCT01403766

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
renal transplant patient aged 1 to <19 years old
Descrizione

ID.1

Tipo di dati

boolean

stable allograft function (no history of biopsy proven acute rejection or increase of creatinine of > 10% from baseline in the past 6 months)
Descrizione

ID.2

Tipo di dati

boolean

no changes in maintenance immunosuppression in the month before the protocol biopsy
Descrizione

ID.3

Tipo di dati

boolean

subject and/or parent must be able to understand and provide informed consent
Descrizione

ID.4

Tipo di dati

boolean

Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
biopsy proven acute rejection in the past 6 months
Descrizione

ID.5

Tipo di dati

boolean

change in maintenance immunosuppression in the month before the protocol biopsy
Descrizione

ID.6

Tipo di dati

boolean

known diabetes mellitus
Descrizione

ID.7

Tipo di dati

boolean

known thyroid dysfunction
Descrizione

ID.8

Tipo di dati

boolean

allergy to iohexol or other contrast media
Descrizione

ID.9

Tipo di dati

boolean

inability or unwillingness of a participant or their legal guardian to give written informed consent or comply with the study protocol
Descrizione

ID.10

Tipo di dati

boolean

Similar models

Eligibility Chronic Kidney Disease NCT01403766

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
renal transplant patient aged 1 to <19 years old
boolean
ID.2
Item
stable allograft function (no history of biopsy proven acute rejection or increase of creatinine of > 10% from baseline in the past 6 months)
boolean
ID.3
Item
no changes in maintenance immunosuppression in the month before the protocol biopsy
boolean
ID.4
Item
subject and/or parent must be able to understand and provide informed consent
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
biopsy proven acute rejection in the past 6 months
boolean
ID.6
Item
change in maintenance immunosuppression in the month before the protocol biopsy
boolean
ID.7
Item
known diabetes mellitus
boolean
ID.8
Item
known thyroid dysfunction
boolean
ID.9
Item
allergy to iohexol or other contrast media
boolean
ID.10
Item
inability or unwillingness of a participant or their legal guardian to give written informed consent or comply with the study protocol
boolean