ID

13005

Description

A Safety Clinical Trial of Different Doses of MEDI-507 in the Prevention of Acute Renal Allograft Rejection; ODM derived from: https://clinicaltrials.gov/show/NCT00807794

Link

https://clinicaltrials.gov/show/NCT00807794

Keywords

  1. 1/11/16 1/11/16 -
Copyright Holder

CC BY-NC 3.0

Uploaded on

January 11, 2016

DOI

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License

Creative Commons BY-NC 3.0

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Eligibility Kidney Diseases NCT00807794

Eligibility Kidney Diseases NCT00807794

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
renal allograft recipients receiving their first or second allograft
Description

renal allograft recipients

Data type

boolean

Alias
UMLS CUI [1]
C0564454
age over 18
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
maintained on conventional immunosuppression
Description

immunosuppression

Data type

boolean

Alias
UMLS CUI [1]
C0021079
completed informed consent document
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
known hypersensitivity to medi-507
Description

hypersensitivity to medi-507

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C1310928
more than two renal allografts
Description

more than two renal allografts

Data type

boolean

Alias
UMLS CUI [1]
C0564454
moribund and unlikely (in the opinion of the investigator) to survive the duration of the trial
Description

life expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
simultaneous use of other investigational agents (this does not include the use of licensed agents for indications not listed in the package insert)
Description

investigational agents

Data type

boolean

Alias
UMLS CUI [1]
C1875319
pregnancy or nursing mother: ø human immunodeficiency virus infection ø hemodialysis or chronic peritoneal dialysis ø use of a ventilator ø hyperacute rejection
Description

pregnancy or nursing mother: ø human immunodeficiency virus infection ø hemodialysis or chronic peritoneal dialysis ø use of a ventilator ø hyperacute rejection

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0019682
UMLS CUI [3]
C0011946
UMLS CUI [4]
C0087153
UMLS CUI [5]
C0301947
having received okt3, tacrolimus, or antilymphocyte globulin during the current allograft
Description

okt3, tacrolimus, or antilymphocyte globulin

Data type

boolean

Alias
UMLS CUI [1]
C0085379
UMLS CUI [2]
C0085149
UMLS CUI [3]
C0003370
less than 10 ml/hr average urine output over 4 hours since the end of surgery
Description

urine output

Data type

boolean

Alias
UMLS CUI [1]
C1287298

Similar models

Eligibility Kidney Diseases NCT00807794

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
renal allograft recipients
Item
renal allograft recipients receiving their first or second allograft
boolean
C0564454 (UMLS CUI [1])
age
Item
age over 18
boolean
C0001779 (UMLS CUI [1])
immunosuppression
Item
maintained on conventional immunosuppression
boolean
C0021079 (UMLS CUI [1])
informed consent
Item
completed informed consent document
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
hypersensitivity to medi-507
Item
known hypersensitivity to medi-507
boolean
C0020517 (UMLS CUI [1,1])
C1310928 (UMLS CUI [1,2])
more than two renal allografts
Item
more than two renal allografts
boolean
C0564454 (UMLS CUI [1])
life expectancy
Item
moribund and unlikely (in the opinion of the investigator) to survive the duration of the trial
boolean
C0023671 (UMLS CUI [1])
investigational agents
Item
simultaneous use of other investigational agents (this does not include the use of licensed agents for indications not listed in the package insert)
boolean
C1875319 (UMLS CUI [1])
pregnancy or nursing mother: ø human immunodeficiency virus infection ø hemodialysis or chronic peritoneal dialysis ø use of a ventilator ø hyperacute rejection
Item
pregnancy or nursing mother: ø human immunodeficiency virus infection ø hemodialysis or chronic peritoneal dialysis ø use of a ventilator ø hyperacute rejection
boolean
C0032961 (UMLS CUI [1])
C0019682 (UMLS CUI [2])
C0011946 (UMLS CUI [3])
C0087153 (UMLS CUI [4])
C0301947 (UMLS CUI [5])
okt3, tacrolimus, or antilymphocyte globulin
Item
having received okt3, tacrolimus, or antilymphocyte globulin during the current allograft
boolean
C0085379 (UMLS CUI [1])
C0085149 (UMLS CUI [2])
C0003370 (UMLS CUI [3])
urine output
Item
less than 10 ml/hr average urine output over 4 hours since the end of surgery
boolean
C1287298 (UMLS CUI [1])

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