ID

14141

Beschrijving

Comparison of Two Biphasic Insulin Aspart Treatments in Subjects With Type 2 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT01520753

Link

https://clinicaltrials.gov/show/NCT01520753

Trefwoorden

  1. 31-03-16 31-03-16 -
Geüploaded op

31 maart 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Diabetes NCT01520753

Eligibility Diabetes NCT01520753

  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT01520753
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 2 diabetes
Beschrijving

Type 2 diabetes

Datatype

boolean

Alias
UMLS CUI [1]
C0011860
duration of diabetes for longer than 12 months
Beschrijving

Duration of diabetes

Datatype

boolean

Alias
UMLS CUI [1,1]
C0872146
UMLS CUI [1,2]
C0011860
body mass index (bmi) below 35.0 kg/m^2
Beschrijving

ID.3

Datatype

boolean

hba1c below 11.0 %
Beschrijving

Hba1c

Datatype

boolean

Alias
UMLS CUI [1]
C0019018
treatment with bhi (biphasic human insulin) 20 or 30 twice daily for at least three months and in the last month as sole anti-diabetic treatment (i.e., no additional oral hypoglycaemic medication or daily use of short-acting insulin supplement)
Beschrijving

Biphasic human insulin and insulin regime

Datatype

boolean

Alias
UMLS CUI [1]
C1562202
UMLS CUI [2]
C0557978
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
current treatment with agents affecting glucose metabolism
Beschrijving

Pharmacotherapy interferes with blood glucose level

Datatype

boolean

Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0392201
history of drug or alcohol dependence
Beschrijving

Substance use disorder

Datatype

boolean

Alias
UMLS CUI [1]
C0038586
impaired hepatic function
Beschrijving

Hepatic function

Datatype

boolean

Alias
UMLS CUI [1]
C0232741
impaired renal function
Beschrijving

Renal function

Datatype

boolean

Alias
UMLS CUI [1]
C0232804
cardiac disease
Beschrijving

Cardiac disease

Datatype

boolean

Alias
UMLS CUI [1]
C0018799
proliferative retinopathy
Beschrijving

Proliferative retinopathy

Datatype

boolean

Alias
UMLS CUI [1]
C0339467
recurrent severe hypoglycaemia or advanced neuropathy
Beschrijving

Recurrent severe hypoglycaemia or neuropathy

Datatype

boolean

Alias
UMLS CUI [1]
C0342316
UMLS CUI [2]
C0442874

Similar models

Eligibility Diabetes NCT01520753

  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT01520753
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Type 2 diabetes
Item
type 2 diabetes
boolean
C0011860 (UMLS CUI [1])
Duration of diabetes
Item
duration of diabetes for longer than 12 months
boolean
C0872146 (UMLS CUI [1,1])
C0011860 (UMLS CUI [1,2])
ID.3
Item
body mass index (bmi) below 35.0 kg/m^2
boolean
Hba1c
Item
hba1c below 11.0 %
boolean
C0019018 (UMLS CUI [1])
Biphasic human insulin and insulin regime
Item
treatment with bhi (biphasic human insulin) 20 or 30 twice daily for at least three months and in the last month as sole anti-diabetic treatment (i.e., no additional oral hypoglycaemic medication or daily use of short-acting insulin supplement)
boolean
C1562202 (UMLS CUI [1])
C0557978 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Pharmacotherapy interferes with blood glucose level
Item
current treatment with agents affecting glucose metabolism
boolean
C0013216 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0392201 (UMLS CUI [1,3])
Substance use disorder
Item
history of drug or alcohol dependence
boolean
C0038586 (UMLS CUI [1])
Hepatic function
Item
impaired hepatic function
boolean
C0232741 (UMLS CUI [1])
Renal function
Item
impaired renal function
boolean
C0232804 (UMLS CUI [1])
Cardiac disease
Item
cardiac disease
boolean
C0018799 (UMLS CUI [1])
Proliferative retinopathy
Item
proliferative retinopathy
boolean
C0339467 (UMLS CUI [1])
Recurrent severe hypoglycaemia or neuropathy
Item
recurrent severe hypoglycaemia or advanced neuropathy
boolean
C0342316 (UMLS CUI [1])
C0442874 (UMLS CUI [2])

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