ID

34266

Beskrivning

The Norwegian Pancreas Transplantation (PTx) Study; ODM derived from: https://clinicaltrials.gov/show/NCT01957696

Länk

https://clinicaltrials.gov/show/NCT01957696

Nyckelord

  1. 2019-01-16 2019-01-16 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

16 januari 2019

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus NCT01957696

Eligibility Diabetes Mellitus NCT01957696

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
age ≥18 years
Beskrivning

ID.1

Datatyp

boolean

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

ID.2

Datatyp

boolean

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

ID.3

Datatyp

boolean

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

ID.4

Datatyp

boolean

signed and dated informed consent form.
Beskrivning

ID.5

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
evidence of systemic infection
Beskrivning

ID.6

Datatyp

boolean

presence of unstable cardiovascular disease.
Beskrivning

ID.7

Datatyp

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).
Beskrivning

ID.8

Datatyp

boolean

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

ID.9

Datatyp

boolean

any positive test for hbv, hbc or hiv.
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Diabetes Mellitus NCT01957696

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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

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