ID

15746

Beskrivning

Glycemic Control of Biphasic Insulin Aspart 30 in Type 2 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT01697631

Länk

https://clinicaltrials.gov/show/NCT01697631

Nyckelord

  1. 2016-06-10 2016-06-10 -
Uppladdad den

10 juni 2016

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Diabetes NCT01697631

Eligibility Diabetes NCT01697631

  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT01697631
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 2 diabetes
Beskrivning

type 2 diabetes

Datatyp

boolean

Alias
UMLS CUI [1]
C0011860
current treatment with conventional biphasic human insulin 30/70 b.i.d. (twice daily) for at least 3 months
Beskrivning

conventional biphasic human insulin

Datatyp

boolean

Alias
UMLS CUI [1]
C0356369
hba1c (glycosylated haemoglobin) equal to or below 12%
Beskrivning

hba1c

Datatyp

boolean

Alias
UMLS CUI [1]
C0019018
willing and able to perform self blood glucose monitoring (smbg)
Beskrivning

self blood glucose monitoring

Datatyp

boolean

Alias
UMLS CUI [1]
C0005803
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of drug or alcohol dependence
Beskrivning

drug or alcohol dependence

Datatyp

boolean

Alias
UMLS CUI [1]
C0038586
mental incapacity, unwillingness or language barriers precluding adequate understanding or co-operation
Beskrivning

language barriers

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0162340
previous participation in this trial
Beskrivning

previous participation in this trial

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
receipt of any investigational drug within the last month prior to this trial
Beskrivning

investigational drug

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
known or suspected allergy to trial products or related products
Beskrivning

allergy to trial products

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C3854006

Similar models

Eligibility Diabetes NCT01697631

  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT01697631
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
type 2 diabetes
Item
type 2 diabetes
boolean
C0011860 (UMLS CUI [1])
conventional biphasic human insulin
Item
current treatment with conventional biphasic human insulin 30/70 b.i.d. (twice daily) for at least 3 months
boolean
C0356369 (UMLS CUI [1])
hba1c
Item
hba1c (glycosylated haemoglobin) equal to or below 12%
boolean
C0019018 (UMLS CUI [1])
self blood glucose monitoring
Item
willing and able to perform self blood glucose monitoring (smbg)
boolean
C0005803 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
drug or alcohol dependence
Item
history of drug or alcohol dependence
boolean
C0038586 (UMLS CUI [1])
language barriers
Item
mental incapacity, unwillingness or language barriers precluding adequate understanding or co-operation
boolean
C0021430 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0162340 (UMLS CUI [1,3])
previous participation in this trial
Item
previous participation in this trial
boolean
C2348568 (UMLS CUI [1])
investigational drug
Item
receipt of any investigational drug within the last month prior to this trial
boolean
C2348568 (UMLS CUI [1])
allergy to trial products
Item
known or suspected allergy to trial products or related products
boolean
C0020517 (UMLS CUI [1,1])
C3854006 (UMLS CUI [1,2])

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