Eligibility Diabetes Mellitus NCT01957696

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
age ≥18 years
Descrizione

ID.1

Tipo di dati

boolean

patients who receive a primary or secondary pancreas transplant, with or without a simultaneous kidney transplant (spk).
Descrizione

ID.2

Tipo di dati

boolean

women who are of childbearing potential must have a negative serum pregnancy test at baseline.
Descrizione

ID.3

Tipo di dati

boolean

operability has to be ascertained by preoperative examination, performed by nephrologist, transplant surgeon and anaesthesiologist.
Descrizione

ID.4

Tipo di dati

boolean

signed and dated informed consent form.
Descrizione

ID.5

Tipo di dati

boolean

Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
evidence of systemic infection
Descrizione

ID.6

Tipo di dati

boolean

presence of unstable cardiovascular disease.
Descrizione

ID.7

Tipo di dati

boolean

malignancy < 5 years prior to entry into the trial (with the exception of adequately treated basal cell or squamous cell carcinomas of the skin).
Descrizione

ID.8

Tipo di dati

boolean

panel-reactive antibodies (pra) > 20% or the presence of donor-specific antigens (dsa).
Descrizione

ID.9

Tipo di dati

boolean

any positive test for hbv, hbc or hiv.
Descrizione

ID.10

Tipo di dati

boolean

Similar models

Eligibility Diabetes Mellitus NCT01957696

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
age ≥18 years
boolean
ID.2
Item
patients who receive a primary or secondary pancreas transplant, with or without a simultaneous kidney transplant (spk).
boolean
ID.3
Item
women who are of childbearing potential must have a negative serum pregnancy test at baseline.
boolean
ID.4
Item
operability has to be ascertained by preoperative examination, performed by nephrologist, transplant surgeon and anaesthesiologist.
boolean
ID.5
Item
signed and dated informed consent form.
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
evidence of systemic infection
boolean
ID.7
Item
presence of unstable cardiovascular disease.
boolean
ID.8
Item
malignancy < 5 years prior to entry into the trial (with the exception of adequately treated basal cell or squamous cell carcinomas of the skin).
boolean
ID.9
Item
panel-reactive antibodies (pra) > 20% or the presence of donor-specific antigens (dsa).
boolean
ID.10
Item
any positive test for hbv, hbc or hiv.
boolean