ID

34197

Beschrijving

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

Link

https://clinicaltrials.gov/show/NCT01403766

Trefwoorden

  1. 15-01-19 15-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

15 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Chronic Kidney Disease NCT01403766

Eligibility Chronic Kidney Disease NCT01403766

Inclusion Criteria
Beschrijving

Inclusion Criteria

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

ID.1

Datatype

boolean

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

ID.2

Datatype

boolean

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

ID.3

Datatype

boolean

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

ID.4

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

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

ID.5

Datatype

boolean

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

ID.6

Datatype

boolean

known diabetes mellitus
Beschrijving

ID.7

Datatype

boolean

known thyroid dysfunction
Beschrijving

ID.8

Datatype

boolean

allergy to iohexol or other contrast media
Beschrijving

ID.9

Datatype

boolean

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

ID.10

Datatype

boolean

Similar models

Eligibility Chronic Kidney Disease NCT01403766

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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