ID

31397

Beschrijving

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

Link

https://clinicaltrials.gov/show/NCT00980356

Trefwoorden

Versies (1)
  1. 19-08-18 19-08-18 -
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see clinicaltrials.gov

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19 augustus 2018

DOI

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Creative Commons BY 4.0
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Eligibility Diabetes Mellitus NCT00980356

Engels

Eligibility Diabetes Mellitus NCT00980356

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

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

New Onset Diabetes After Transplant; Glucose tolerance test; Pathologic

Datatype

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.
Beschrijving

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

Datatype

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.
Beschrijving

Graft material; Stable status; Duration (temporal concept)

Datatype

boolean

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

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

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

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

Datatype

boolean

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

Body mass index

Datatype

boolean

Alias
UMLS CUI [1]
C1305855
pregnancy
Beschrijving

Pregnancy

Datatype

boolean

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

Renal Insufficiency; Severe (severity modifier)

Datatype

boolean

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

Hepatic impairment; Severe (severity modifier)

Datatype

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%
Beschrijving

Plasma Glucose Measurement; Elevation; Severe (severity modifier)

Datatype

boolean

Alias
UMLS CUI [1,1]
C0202042
UMLS CUI [1,2]
C0702240
UMLS CUI [1,3]
C0205082
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Similar models

Eligibility Diabetes Mellitus NCT00980356

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])
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