ID

17201

Description

Efficacy and Safety of Vildagliptin in Combination With Glimepiride in Patients With Type 2 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT00099944

Link

https://clinicaltrials.gov/show/NCT00099944

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 NCT00099944

Eligibility Diabetes Mellitus, Type 2 NCT00099944

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
previously treated with a sulfonylurea for at least 3 months
Description

Sulfonylurea

Data type

boolean

Alias
UMLS CUI [1]
C0038766
body mass index (bmi) in the range 22-45
Description

Body mass index

Data type

boolean

Alias
UMLS CUI [1]
C1305855
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
type 1 diabetes
Description

Diabetes Mellitus, Insulin-Dependent

Data type

boolean

Alias
UMLS CUI [1]
C0011854
pregnancy or lactation
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
evidence of serious cardiovascular complications
Description

Cardiac complication Serious Evidence of

Data type

boolean

Alias
UMLS CUI [1,1]
C0161816
UMLS CUI [1,2]
C0205404
UMLS CUI [1,3]
C0332120
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
laboratory value abnormalities as defined by the protocol
Description

Laboratory test result abnormal

Data type

boolean

Alias
UMLS CUI [1]
C0438215
known sensitivity to glimepiride
Description

Sensitivity glimepiride

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0061323
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 NCT00099944

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])
Sulfonylurea
Item
previously treated with a sulfonylurea for at least 3 months
boolean
C0038766 (UMLS CUI [1])
Body mass index
Item
body mass index (bmi) in the range 22-45
boolean
C1305855 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Diabetes Mellitus, Insulin-Dependent
Item
type 1 diabetes
boolean
C0011854 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnancy or lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Cardiac complication Serious Evidence of
Item
evidence of serious cardiovascular complications
boolean
C0161816 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0332120 (UMLS CUI [1,3])
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])
Laboratory test result abnormal
Item
laboratory value abnormalities as defined by the protocol
boolean
C0438215 (UMLS CUI [1])
Sensitivity glimepiride
Item
known sensitivity to glimepiride
boolean
C0020517 (UMLS CUI [1,1])
C0061323 (UMLS CUI [1,2])
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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