Eligibility Prostate Cancer NCT00922129

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
male patients ≤ 50 years in their post renal transplant follow-up;
Descrizione

ID.1

Tipo di dati

boolean

biopsy confirmed prostate cancer;
Descrizione

ID.2

Tipo di dati

boolean

stable renal function with gfr ≥ 40 ml/min.
Descrizione

ID.3

Tipo di dati

boolean

Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with metastatic disease;
Descrizione

ID.4

Tipo di dati

boolean

uncontrolled hyperlipidemia;
Descrizione

ID.5

Tipo di dati

boolean

proteinuria > 500 mg/day;
Descrizione

ID.6

Tipo di dati

boolean

biopsy evidence of acute rejection within the past 3 months;
Descrizione

ID.7

Tipo di dati

boolean

existence of any surgical or medical condition, other than the current transplant, which in the opinion of the investigator might significantly alter the absorption, distribution, metabolism or excretion of study medication;
Descrizione

ID.8

Tipo di dati

boolean

patients with mental illness;
Descrizione

ID.9

Tipo di dati

boolean

inability to cooperate or communicate with the investigator or unable to complete self administered questionnaires.
Descrizione

ID.10

Tipo di dati

boolean

Similar models

Eligibility Prostate Cancer NCT00922129

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
male patients ≤ 50 years in their post renal transplant follow-up;
boolean
ID.2
Item
biopsy confirmed prostate cancer;
boolean
ID.3
Item
stable renal function with gfr ≥ 40 ml/min.
boolean
Item Group
C0680251 (UMLS CUI)
ID.4
Item
patients with metastatic disease;
boolean
ID.5
Item
uncontrolled hyperlipidemia;
boolean
ID.6
Item
proteinuria > 500 mg/day;
boolean
ID.7
Item
biopsy evidence of acute rejection within the past 3 months;
boolean
ID.8
Item
existence of any surgical or medical condition, other than the current transplant, which in the opinion of the investigator might significantly alter the absorption, distribution, metabolism or excretion of study medication;
boolean
ID.9
Item
patients with mental illness;
boolean
ID.10
Item
inability to cooperate or communicate with the investigator or unable to complete self administered questionnaires.
boolean