ID

34197

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT01403766

Nyckelord

  1. 2019-01-15 2019-01-15 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

15 januari 2019

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Chronic Kidney Disease NCT01403766

Eligibility Chronic Kidney Disease NCT01403766

Inclusion Criteria
Beskrivning

Inclusion Criteria

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

ID.1

Datatyp

boolean

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

ID.2

Datatyp

boolean

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

ID.3

Datatyp

boolean

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

ID.4

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

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

ID.5

Datatyp

boolean

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

ID.6

Datatyp

boolean

known diabetes mellitus
Beskrivning

ID.7

Datatyp

boolean

known thyroid dysfunction
Beskrivning

ID.8

Datatyp

boolean

allergy to iohexol or other contrast media
Beskrivning

ID.9

Datatyp

boolean

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

ID.10

Datatyp

boolean

Similar models

Eligibility Chronic Kidney Disease NCT01403766

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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