ID
13005
Beschrijving
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
Trefwoorden
Versies (1)
- 11-01-16 11-01-16 -
Houder van rechten
CC BY-NC 3.0
Geüploaded op
11 januari 2016
DOI
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Licentie
Creative Commons BY-NC 3.0
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Eligibility Kidney Diseases NCT00807794
Eligibility Kidney Diseases NCT00807794
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
hypersensitivity to medi-507
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C1310928
Beschrijving
more than two renal allografts
Datatype
boolean
Alias
- UMLS CUI [1]
- C0564454
Beschrijving
life expectancy
Datatype
boolean
Alias
- UMLS CUI [1]
- C0023671
Beschrijving
investigational agents
Datatype
boolean
Alias
- UMLS CUI [1]
- C1875319
Beschrijving
pregnancy or nursing mother: ø human immunodeficiency virus infection ø hemodialysis or chronic peritoneal dialysis ø use of a ventilator ø hyperacute rejection
Datatype
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0019682
- UMLS CUI [3]
- C0011946
- UMLS CUI [4]
- C0087153
- UMLS CUI [5]
- C0301947
Beschrijving
okt3, tacrolimus, or antilymphocyte globulin
Datatype
boolean
Alias
- UMLS CUI [1]
- C0085379
- UMLS CUI [2]
- C0085149
- UMLS CUI [3]
- C0003370
Beschrijving
urine output
Datatype
boolean
Alias
- UMLS CUI [1]
- C1287298
Similar models
Eligibility Kidney Diseases NCT00807794
- StudyEvent: Eligibility
C1310928 (UMLS CUI [1,2])
C0019682 (UMLS CUI [2])
C0011946 (UMLS CUI [3])
C0087153 (UMLS CUI [4])
C0301947 (UMLS CUI [5])
C0085149 (UMLS CUI [2])
C0003370 (UMLS CUI [3])