ID

34197

Descripción

Comparison of Markers of Kidney Function; ODM derived from: https://clinicaltrials.gov/show/NCT01403766

Link

https://clinicaltrials.gov/show/NCT01403766

Palabras clave

  1. 15/1/19 15/1/19 -
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

15 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Chronic Kidney Disease NCT01403766

Eligibility Chronic Kidney Disease NCT01403766

Inclusion Criteria
Descripción

Inclusion Criteria

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

ID.1

Tipo de datos

boolean

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

ID.2

Tipo de datos

boolean

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

ID.3

Tipo de datos

boolean

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

ID.4

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

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

ID.5

Tipo de datos

boolean

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

ID.6

Tipo de datos

boolean

known diabetes mellitus
Descripción

ID.7

Tipo de datos

boolean

known thyroid dysfunction
Descripción

ID.8

Tipo de datos

boolean

allergy to iohexol or other contrast media
Descripción

ID.9

Tipo de datos

boolean

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

ID.10

Tipo de datos

boolean

Similar models

Eligibility Chronic Kidney Disease NCT01403766

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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

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