ID

15779

Description

Angiotensin II Blockade for Chronic Allograft Nephropathy; ODM derived from: https://clinicaltrials.gov/show/NCT00067990

Link

https://clinicaltrials.gov/show/NCT00067990

Keywords

Versions (1)
  1. 6/13/16 6/13/16 -
Uploaded on

June 13, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Kidney Disease NCT00067990

English

Eligibility Kidney Disease NCT00067990

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age > 18 years.
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
recipients of a first or a second renal transplant alone or in combination with a pancreas transplantation.
Description

renal transplant

Data type

boolean

Alias
UMLS CUI [1]
C0022671
informed consent
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
adequate baseline biopsy; at least 10 cortical projection fields.
Description

adequate baseline biopsy

Data type

boolean

Alias
UMLS CUI [1]
C0005558
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
age < 18 years.
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
serum creatinine 2.5mg/dl.
Description

serum creatinine

Data type

boolean

Alias
UMLS CUI [1]
C0201976
persistent hyperkalemia; potassium > 5.4 meq/l.
Description

hyperkalemia

Data type

boolean

Alias
UMLS CUI [1]
C0020461
known hypersensitivity to losartan or iodine allergy.
Description

hypersensitivity

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0126174
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0021968
documented renal artery stenosis by duplex ultrasonography.
Description

renal artery stenosis

Data type

boolean

Alias
UMLS CUI [1]
C0035067
UMLS CUI [2]
C3825392
recipients of grafts from an hla-identical sibling.
Description

hla-identical sibling

Data type

boolean

Alias
UMLS CUI [1,1]
C0019633
UMLS CUI [1,2]
C1960320
recipients whose primary renal disease is primary hyperoxaluria,dense-deposit disease, focal segmental glomerulosclerosis or hemolytic uremic syndrome.
Description

primary renal disease

Data type

boolean

Alias
UMLS CUI [1]
C0020501
UMLS CUI [2]
C0403426
UMLS CUI [3]
C0019061
women of childbearing age who wish to become pregnant and/or are unwilling to use contraceptive measures or who are pregnant.
Description

pregnancy and contraceptive methods

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0700589
recipients requiring ace inhibitors or aii blockers for a cardiovascular indication (e.g. systolic dysfunction).
Description

ace inhibitors

Data type

boolean

Alias
UMLS CUI [1]
C0003015
UMLS CUI [2]
C0521942
recipients who are > 55 years old and had a history of cardiovascular disease (coronary artery disease, stroke or peripheral vascular disease).
Description

cardiovascular disease

Data type

boolean

Alias
UMLS CUI [1]
C1956346
UMLS CUI [2]
C0038454
UMLS CUI [3]
C0085096
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Similar models

Eligibility Kidney Disease NCT00067990

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
age > 18 years.
boolean
C0001779 (UMLS CUI [1])
renal transplant
Item
recipients of a first or a second renal transplant alone or in combination with a pancreas transplantation.
boolean
C0022671 (UMLS CUI [1])
informed consent
Item
informed consent
boolean
C0021430 (UMLS CUI [1])
adequate baseline biopsy
Item
adequate baseline biopsy; at least 10 cortical projection fields.
boolean
C0005558 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
age
Item
age < 18 years.
boolean
C0001779 (UMLS CUI [1])
serum creatinine
Item
serum creatinine 2.5mg/dl.
boolean
C0201976 (UMLS CUI [1])
hyperkalemia
Item
persistent hyperkalemia; potassium > 5.4 meq/l.
boolean
C0020461 (UMLS CUI [1])
hypersensitivity
Item
known hypersensitivity to losartan or iodine allergy.
boolean
C0020517 (UMLS CUI [1,1])
C0126174 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0021968 (UMLS CUI [2,2])
renal artery stenosis
Item
documented renal artery stenosis by duplex ultrasonography.
boolean
C0035067 (UMLS CUI [1])
C3825392 (UMLS CUI [2])
hla-identical sibling
Item
recipients of grafts from an hla-identical sibling.
boolean
C0019633 (UMLS CUI [1,1])
C1960320 (UMLS CUI [1,2])
primary renal disease
Item
recipients whose primary renal disease is primary hyperoxaluria,dense-deposit disease, focal segmental glomerulosclerosis or hemolytic uremic syndrome.
boolean
C0020501 (UMLS CUI [1])
C0403426 (UMLS CUI [2])
C0019061 (UMLS CUI [3])
pregnancy and contraceptive methods
Item
women of childbearing age who wish to become pregnant and/or are unwilling to use contraceptive measures or who are pregnant.
boolean
C0032961 (UMLS CUI [1])
C0700589 (UMLS CUI [2])
ace inhibitors
Item
recipients requiring ace inhibitors or aii blockers for a cardiovascular indication (e.g. systolic dysfunction).
boolean
C0003015 (UMLS CUI [1])
C0521942 (UMLS CUI [2])
cardiovascular disease
Item
recipients who are > 55 years old and had a history of cardiovascular disease (coronary artery disease, stroke or peripheral vascular disease).
boolean
C1956346 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C0085096 (UMLS CUI [3])
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