ID

17301

Beskrivning

Efficacy and Safety of Biphasic Insulin Aspart 30 FlexPen® in Insulin Naive Subjects With Type 2 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT00600366

Länk

https://clinicaltrials.gov/show/NCT00600366

Nyckelord

Versioner (1)
  1. 2016-09-05 2016-09-05 -
Uppladdad den

5 september 2016

DOI

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Licens

Creative Commons BY 4.0
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Eligibility Diabetes NCT00600366

Engelsk

Eligibility Diabetes NCT00600366

1 Formulär  
  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT00600366
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 2 diabetes
Beskrivning

Diabetes Mellitus, Non-Insulin-Dependent

Datatyp

boolean

Alias
UMLS CUI [1]
C0011860
insulin naive diabetes
Beskrivning

Insulin Therapy naive Diabetes

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0021641
UMLS CUI [1,2]
C0919936
UMLS CUI [1,3]
C0011847
current treatment with oha, secondary failure
Beskrivning

Oral hypoglycemic Therapeutic procedure failed secondary

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0359086
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C0231175
UMLS CUI [1,4]
C0205436
body mass index (bmi) below 40 kg/m2
Beskrivning

Body mass index

Datatyp

boolean

Alias
UMLS CUI [1]
C1305855
hba1c over 8.5%
Beskrivning

Glycosylated hemoglobin A

Datatyp

boolean

Alias
UMLS CUI [1]
C0019018
willing and able to start with insulin therapy and to perform self-blood glucose monitoring
Beskrivning

Insulin regime Willing | Blood Glucose Self-Monitoring Willing

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0557978
UMLS CUI [1,2]
C0600109
UMLS CUI [2,1]
C0005803
UMLS CUI [2,2]
C0600109
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of drug or alcohol abuse
Beskrivning

Substance Use Disorders

Datatyp

boolean

Alias
UMLS CUI [1]
C0038586
receipt of the investigational drug within the last month prior to this trial
Beskrivning

Investigational New Drugs

Datatyp

boolean

Alias
UMLS CUI [1]
C0013230
known or suspected allergy to trial products or related products
Beskrivning

Hypersensitivity Investigational New Drugs | Hypersensitivity Pharmaceutical Preparations Related Investigational New Drugs

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013230
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0013227
UMLS CUI [2,3]
C0439849
UMLS CUI [2,4]
C0013230
severe uncontrolled hypertension
Beskrivning

Uncontrolled hypertension Severe

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1868885
UMLS CUI [1,2]
C0205082
any disease or condition, which the investigator feels, would interfere with the trial
Beskrivning

Disease Interferes with Clinical Trial | Condition Interferes with Clinical Trial

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0008976
UMLS CUI [2,1]
C0348080
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0008976
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Similar models

Eligibility Diabetes NCT00600366

1 Formulär
  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT00600366
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus, Non-Insulin-Dependent
Item
type 2 diabetes
boolean
C0011860 (UMLS CUI [1])
Insulin Therapy naive Diabetes
Item
insulin naive diabetes
boolean
C0021641 (UMLS CUI [1,1])
C0919936 (UMLS CUI [1,2])
C0011847 (UMLS CUI [1,3])
Oral hypoglycemic Therapeutic procedure failed secondary
Item
current treatment with oha, secondary failure
boolean
C0359086 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
C0205436 (UMLS CUI [1,4])
Body mass index
Item
body mass index (bmi) below 40 kg/m2
boolean
C1305855 (UMLS CUI [1])
Glycosylated hemoglobin A
Item
hba1c over 8.5%
boolean
C0019018 (UMLS CUI [1])
Insulin regime Willing | Blood Glucose Self-Monitoring Willing
Item
willing and able to start with insulin therapy and to perform self-blood glucose monitoring
boolean
C0557978 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
C0005803 (UMLS CUI [2,1])
C0600109 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Substance Use Disorders
Item
history of drug or alcohol abuse
boolean
C0038586 (UMLS CUI [1])
Investigational New Drugs
Item
receipt of the investigational drug within the last month prior to this trial
boolean
C0013230 (UMLS CUI [1])
Hypersensitivity Investigational New Drugs | Hypersensitivity Pharmaceutical Preparations Related Investigational New Drugs
Item
known or suspected allergy to trial products or related products
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0013227 (UMLS CUI [2,2])
C0439849 (UMLS CUI [2,3])
C0013230 (UMLS CUI [2,4])
Uncontrolled hypertension Severe
Item
severe uncontrolled hypertension
boolean
C1868885 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Disease Interferes with Clinical Trial | Condition Interferes with Clinical Trial
Item
any disease or condition, which the investigator feels, would interfere with the trial
boolean
C0012634 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0348080 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0008976 (UMLS CUI [2,3])
Tillbaka till toppen 

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