ID

34591

Description

Evaluation of the Effect of Gemigliptin on Metabolic Endotoxemia and Lipemia Induced by High Fat Diet in Patients With Type 2 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT02186080

Link

https://clinicaltrials.gov/show/NCT02186080

Keywords

  1. 1/19/19 1/19/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 19, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Type 2 Diabetes Mellitus NCT02186080

Eligibility Type 2 Diabetes Mellitus NCT02186080

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age from 20 to 75
Description

ID.1

Data type

boolean

at least 6 months from the diagnosis of type 2 diabetes
Description

ID.2

Data type

boolean

current diabetes treatment: life style modification and/or metformin and/or sulfornylurea
Description

ID.3

Data type

boolean

no change of the diabetes treatment (drug number and dossage) in recent 3 months
Description

ID.4

Data type

boolean

hba1c 6.5% to 10%
Description

ID.5

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
recent cardiovascular event in 6 months
Description

ID.6

Data type

boolean

concurrent use of statin or fibrate or ezetimibe
Description

ID.7

Data type

boolean

renal failure, chronic liver disease
Description

ID.8

Data type

boolean

pregnancy or lactation
Description

ID.9

Data type

boolean

use of other dpp-4 inhibitor or glp-1 analogue in recent 3 months
Description

ID.10

Data type

boolean

Similar models

Eligibility Type 2 Diabetes Mellitus NCT02186080

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
age from 20 to 75
boolean
ID.2
Item
at least 6 months from the diagnosis of type 2 diabetes
boolean
ID.3
Item
current diabetes treatment: life style modification and/or metformin and/or sulfornylurea
boolean
ID.4
Item
no change of the diabetes treatment (drug number and dossage) in recent 3 months
boolean
ID.5
Item
hba1c 6.5% to 10%
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
recent cardiovascular event in 6 months
boolean
ID.7
Item
concurrent use of statin or fibrate or ezetimibe
boolean
ID.8
Item
renal failure, chronic liver disease
boolean
ID.9
Item
pregnancy or lactation
boolean
ID.10
Item
use of other dpp-4 inhibitor or glp-1 analogue in recent 3 months
boolean

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