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])
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])