ID

17205

Description

A Clinical Study to Assess the Effect of Vildagliptin on Postprandial Lipid Parameters in Patients With Type 2 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT00099957

Link

https://clinicaltrials.gov/show/NCT00099957

Keywords

  1. 8/31/16 8/31/16 -
Uploaded on

August 31, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus, Type 2 NCT00099957

Eligibility Diabetes Mellitus, Type 2 NCT00099957

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
blood glucose criteria must be met
Description

Blood Glucose criteria Fulfill

Data type

boolean

Alias
UMLS CUI [1,1]
C0005802
UMLS CUI [1,2]
C0243161
UMLS CUI [1,3]
C1550543
genetic markers associated with increased risk of cardiovascular disease
Description

Genetic Markers Associated with High risk of Cardiovascular Disease

Data type

boolean

Alias
UMLS CUI [1,1]
C0017393
UMLS CUI [1,2]
C0332281
UMLS CUI [1,3]
C0332167
UMLS CUI [1,4]
C0007222
not currently on drug therapy for type 2 diabetes
Description

Pharmacotherapy Diabetes Mellitus, Non-Insulin-Dependent

Data type

boolean

Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C0011860
body mass index (bmi) in the range 25-40
Description

Body mass index

Data type

boolean

Alias
UMLS CUI [1]
C1305855
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy or lactation
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
type 1 diabetes
Description

Diabetes Mellitus, Insulin-Dependent

Data type

boolean

Alias
UMLS CUI [1]
C0011854
high cholesterol as defined by the protocol
Description

Hypercholesterolemia

Data type

boolean

Alias
UMLS CUI [1]
C0020443
evidence of serious diabetic complications
Description

Complications of Diabetes Mellitus Serious Evidence of

Data type

boolean

Alias
UMLS CUI [1,1]
C0342257
UMLS CUI [1,2]
C0205404
UMLS CUI [1,3]
C0332120
other protocol-defined exclusion criteria may apply
Description

Exclusion Criteria Study Protocol

Data type

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C2348563

Similar models

Eligibility Diabetes Mellitus, Type 2 NCT00099957

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Blood Glucose criteria Fulfill
Item
blood glucose criteria must be met
boolean
C0005802 (UMLS CUI [1,1])
C0243161 (UMLS CUI [1,2])
C1550543 (UMLS CUI [1,3])
Genetic Markers Associated with High risk of Cardiovascular Disease
Item
genetic markers associated with increased risk of cardiovascular disease
boolean
C0017393 (UMLS CUI [1,1])
C0332281 (UMLS CUI [1,2])
C0332167 (UMLS CUI [1,3])
C0007222 (UMLS CUI [1,4])
Pharmacotherapy Diabetes Mellitus, Non-Insulin-Dependent
Item
not currently on drug therapy for type 2 diabetes
boolean
C0013216 (UMLS CUI [1,1])
C0011860 (UMLS CUI [1,2])
Body mass index
Item
body mass index (bmi) in the range 25-40
boolean
C1305855 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Pregnancy | Breast Feeding
Item
pregnancy or lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Diabetes Mellitus, Insulin-Dependent
Item
type 1 diabetes
boolean
C0011854 (UMLS CUI [1])
Hypercholesterolemia
Item
high cholesterol as defined by the protocol
boolean
C0020443 (UMLS CUI [1])
Complications of Diabetes Mellitus Serious Evidence of
Item
evidence of serious diabetic complications
boolean
C0342257 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0332120 (UMLS CUI [1,3])
Exclusion Criteria Study Protocol
Item
other protocol-defined exclusion criteria may apply
boolean
C0680251 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])

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