ID

31397

Beskrivning

Vildagliptin in New Onset Diabetes After Transplantation; ODM derived from: https://clinicaltrials.gov/show/NCT00980356

Länk

https://clinicaltrials.gov/show/NCT00980356

Nyckelord

Versioner (1)
  1. 2018-08-19 2018-08-19 -
Rättsinnehavare

see clinicaltrials.gov

Uppladdad den

19 augusti 2018

DOI

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Creative Commons BY 4.0
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Eligibility Diabetes Mellitus NCT00980356

Engelsk

Eligibility Diabetes Mellitus NCT00980356

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
• newly diagnosed nodat defined by pathologic ogtt (2h, 75mg glucose): glucose ≥ 200mg/dl
Beskrivning

New Onset Diabetes After Transplant; Glucose tolerance test; Pathologic

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3896643
UMLS CUI [1,2]
C0017741
UMLS CUI [1,3]
C1521733
renal transplantation (deceased or living donor) and treatment with the standard immunosuppression at our center, consisting of triple therapy with tacrolimus or cyclosporine a, mycophenolate mofetil or azathioprine, and prednisone.
Beskrivning

Kidney Transplantation; Cadaver donor (person); Living Donors | Immunosuppression | Tacrolimus | Cyclosporine | mycophenolate mofetil | Azathioprine | Prednisone

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0022671
UMLS CUI [1,2]
C0524354
UMLS CUI [1,3]
C0348050
UMLS CUI [2]
C4048329
UMLS CUI [3]
C0085149
UMLS CUI [4]
C0010592
UMLS CUI [5]
C0209368
UMLS CUI [6]
C0004482
UMLS CUI [7]
C0032952
stable graft function for more than 6 months post transplant.
Beskrivning

Graft material; Stable status; Duration (temporal concept)

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0181074
UMLS CUI [1,2]
C0205360
UMLS CUI [1,3]
C0449238
informed consent of the patient
Beskrivning

Informed Consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with prior history of type 1 or type 2 diabetes
Beskrivning

Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent

Datatyp

boolean

Alias
UMLS CUI [1]
C0011854
UMLS CUI [2]
C0011860
body mass index (bmi) > 40
Beskrivning

Body mass index

Datatyp

boolean

Alias
UMLS CUI [1]
C1305855
pregnancy
Beskrivning

Pregnancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
severe renal impairment (gfr < 30 ml/min./1.73 m2)
Beskrivning

Renal Insufficiency; Severe (severity modifier)

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1565489
UMLS CUI [1,2]
C0205082
severe liver impairment
Beskrivning

Hepatic impairment; Severe (severity modifier)

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0948807
UMLS CUI [1,2]
C0205082
severe blood glucose elevation with the need for therapy with insulin or hba1c >8.5%
Beskrivning

Plasma Glucose Measurement; Elevation; Severe (severity modifier)

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0202042
UMLS CUI [1,2]
C0702240
UMLS CUI [1,3]
C0205082
Tillbaka till toppen

Similar models

Eligibility Diabetes Mellitus NCT00980356

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
New Onset Diabetes After Transplant; Glucose tolerance test; Pathologic
Item
• newly diagnosed nodat defined by pathologic ogtt (2h, 75mg glucose): glucose ≥ 200mg/dl
boolean
C3896643 (UMLS CUI [1,1])
C0017741 (UMLS CUI [1,2])
C1521733 (UMLS CUI [1,3])
Kidney Transplantation; Cadaver donor (person); Living Donors | Immunosuppression | Tacrolimus | Cyclosporine | mycophenolate mofetil | Azathioprine | Prednisone
Item
renal transplantation (deceased or living donor) and treatment with the standard immunosuppression at our center, consisting of triple therapy with tacrolimus or cyclosporine a, mycophenolate mofetil or azathioprine, and prednisone.
boolean
C0022671 (UMLS CUI [1,1])
C0524354 (UMLS CUI [1,2])
C0348050 (UMLS CUI [1,3])
C4048329 (UMLS CUI [2])
C0085149 (UMLS CUI [3])
C0010592 (UMLS CUI [4])
C0209368 (UMLS CUI [5])
C0004482 (UMLS CUI [6])
C0032952 (UMLS CUI [7])
Graft material; Stable status; Duration (temporal concept)
Item
stable graft function for more than 6 months post transplant.
boolean
C0181074 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Informed Consent
Item
informed consent of the patient
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent
Item
patients with prior history of type 1 or type 2 diabetes
boolean
C0011854 (UMLS CUI [1])
C0011860 (UMLS CUI [2])
Body mass index
Item
body mass index (bmi) > 40
boolean
C1305855 (UMLS CUI [1])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Renal Insufficiency; Severe (severity modifier)
Item
severe renal impairment (gfr < 30 ml/min./1.73 m2)
boolean
C1565489 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Hepatic impairment; Severe (severity modifier)
Item
severe liver impairment
boolean
C0948807 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Plasma Glucose Measurement; Elevation; Severe (severity modifier)
Item
severe blood glucose elevation with the need for therapy with insulin or hba1c >8.5%
boolean
C0202042 (UMLS CUI [1,1])
C0702240 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,3])
Tillbaka till toppen 

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