ID

14140

Beschrijving

Comparison of Liraglutide and Glimepiride on Blood Sugar Control in Subjects With Type 2 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT01509755

Link

https://clinicaltrials.gov/show/NCT01509755

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 NCT01509755

Eligibility Diabetes NCT01509755

  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT01509755
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
subjects with type 2 diabetes
Beschrijving

Type 2 Diabetes

Datatype

boolean

Alias
UMLS CUI [1]
C0011860
duration of diabetes at least 3 months
Beschrijving

Duration of Diabtes

Datatype

boolean

Alias
UMLS CUI [1,1]
C0872146
UMLS CUI [1,2]
C0011860
both diet treated and patients in therapy with oha (oral hypoglycemic agents)
Beschrijving

Diabetic diet and oral hypoglycemic agents

Datatype

boolean

Alias
UMLS CUI [1]
C0011878
UMLS CUI [2]
C0359086
body mass index maximum 40 kg/m^2
Beschrijving

Body mass index

Datatype

boolean

Alias
UMLS CUI [1]
C1305855
hba1c based on analysis from central laboratory: between 7.5-10.0%, both inclusive, for diet treated, or maximum 9.0% for oha treated
Beschrijving

Hba1c

Datatype

boolean

Alias
UMLS CUI [1]
C0019018
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
liver or renal disease
Beschrijving

Liver or renal disease

Datatype

boolean

Alias
UMLS CUI [1]
C0023895
UMLS CUI [2]
C0022658
cardiac problems
Beschrijving

Cardiac problems

Datatype

boolean

Alias
UMLS CUI [1]
C0262402
uncontrolled treated/untreated hypertension
Beschrijving

Hypertension

Datatype

boolean

Alias
UMLS CUI [1]
C0020538
proliferative retinopathy
Beschrijving

Proliferative retinopathy

Datatype

boolean

Alias
UMLS CUI [1]
C0339467
recurrent severe hypoglycaemia as judged by the investigator
Beschrijving

Recurrent severe hypoglycaemia

Datatype

boolean

Alias
UMLS CUI [1]
C0342316
known or suspected allergy to trial product or related products
Beschrijving

Allergy to trial product

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C3854006
use of any drug (except for ohas) which in the investigator's opinion could interfere with the blood glucose level
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

Similar models

Eligibility Diabetes NCT01509755

  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT01509755
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Type 2 Diabetes
Item
subjects with type 2 diabetes
boolean
C0011860 (UMLS CUI [1])
Duration of Diabtes
Item
duration of diabetes at least 3 months
boolean
C0872146 (UMLS CUI [1,1])
C0011860 (UMLS CUI [1,2])
Diabetic diet and oral hypoglycemic agents
Item
both diet treated and patients in therapy with oha (oral hypoglycemic agents)
boolean
C0011878 (UMLS CUI [1])
C0359086 (UMLS CUI [2])
Body mass index
Item
body mass index maximum 40 kg/m^2
boolean
C1305855 (UMLS CUI [1])
Hba1c
Item
hba1c based on analysis from central laboratory: between 7.5-10.0%, both inclusive, for diet treated, or maximum 9.0% for oha treated
boolean
C0019018 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Liver or renal disease
Item
liver or renal disease
boolean
C0023895 (UMLS CUI [1])
C0022658 (UMLS CUI [2])
Cardiac problems
Item
cardiac problems
boolean
C0262402 (UMLS CUI [1])
Hypertension
Item
uncontrolled treated/untreated hypertension
boolean
C0020538 (UMLS CUI [1])
Proliferative retinopathy
Item
proliferative retinopathy
boolean
C0339467 (UMLS CUI [1])
Recurrent severe hypoglycaemia
Item
recurrent severe hypoglycaemia as judged by the investigator
boolean
C0342316 (UMLS CUI [1])
Allergy to trial product
Item
known or suspected allergy to trial product or related products
boolean
C0020517 (UMLS CUI [1,1])
C3854006 (UMLS CUI [1,2])
Pharmacotherapy interferes with blood glucose level
Item
use of any drug (except for ohas) which in the investigator's opinion could interfere with the blood glucose level
boolean
C0013216 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0392201 (UMLS CUI [1,3])

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