ID

34201

Description

Paricalcitol Over Inflammatory Parameters on Chronical Kidney Disease Patients; ODM derived from: https://clinicaltrials.gov/show/NCT01820767

Link

https://clinicaltrials.gov/show/NCT01820767

Keywords

  1. 1/15/19 1/15/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 15, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Chronic Kidney Disease NCT01820767

Eligibility Chronic Kidney Disease NCT01820767

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
vd ckd patients using haemodialysis during 3 or more months.
Description

ID.1

Data type

boolean

tunnelized-bearer permanent catheters on haemodialysis at last 6 months previous at the beginning of the study. .
Description

ID.2

Data type

boolean

kt stable, over 45 litres on both sexs.
Description

ID.3

Data type

boolean

patients in treatment wiht atorvastatin
Description

ID.4

Data type

boolean

patients without infectious or inflammatory processes over 8 weeks.
Description

ID.5

Data type

boolean

two consecutive pth < than 400 pg/ml; ca<10.2 and p <7.0 mg/dl.
Description

ID.6

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients > 18 years.
Description

ID.7

Data type

boolean

pregnant women.
Description

ID.8

Data type

boolean

patients hospitalized 4 weeks before the beginning of the treatment.
Description

ID.9

Data type

boolean

immunosuppressor intake.
Description

ID.10

Data type

boolean

Similar models

Eligibility Chronic Kidney Disease NCT01820767

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
vd ckd patients using haemodialysis during 3 or more months.
boolean
ID.2
Item
tunnelized-bearer permanent catheters on haemodialysis at last 6 months previous at the beginning of the study. .
boolean
ID.3
Item
kt stable, over 45 litres on both sexs.
boolean
ID.4
Item
patients in treatment wiht atorvastatin
boolean
ID.5
Item
patients without infectious or inflammatory processes over 8 weeks.
boolean
ID.6
Item
two consecutive pth < than 400 pg/ml; ca<10.2 and p <7.0 mg/dl.
boolean
Item Group
C0680251 (UMLS CUI)
ID.7
Item
patients > 18 years.
boolean
ID.8
Item
pregnant women.
boolean
ID.9
Item
patients hospitalized 4 weeks before the beginning of the treatment.
boolean
ID.10
Item
immunosuppressor intake.
boolean

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