ID

17207

Description

Efficacy and Safety of Vildagliptin Compared to Placebo in Patients With Type 2 Diabetes and Mild Hyperglycemia; ODM derived from: https://clinicaltrials.gov/show/NCT00101712

Lien

https://clinicaltrials.gov/show/NCT00101712

Mots-clés

  1. 31/08/2016 31/08/2016 -
Téléchargé le

31 août 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus, Type 2 NCT00101712

Eligibility Diabetes Mellitus, Type 2 NCT00101712

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
blood glucose criteria must be met
Description

Blood Glucose criteria Fulfill

Type de données

boolean

Alias
UMLS CUI [1,1]
C0005802
UMLS CUI [1,2]
C0243161
UMLS CUI [1,3]
C1550543
not currently on drug therapy for type 2 diabetes
Description

Pharmacotherapy Diabetes Mellitus, Non-Insulin-Dependent

Type de données

boolean

Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C0011860
body mass index (bmi) in the range 22-45
Description

Body mass index

Type de données

boolean

Alias
UMLS CUI [1]
C1305855
diagnosis of type 2 diabetes for at least 8 weeks
Description

Non-Insulin-Dependent Diabetes Mellitus disease length

Type de données

boolean

Alias
UMLS CUI [1,1]
C0011860
UMLS CUI [1,2]
C0872146
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy or lactation
Description

Pregnancy | Breast Feeding

Type de données

boolean

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

Diabetes Mellitus, Insulin-Dependent

Type de données

boolean

Alias
UMLS CUI [1]
C0011854
evidence of serious diabetic complications
Description

Complications of Diabetes Mellitus Serious Evidence of

Type de données

boolean

Alias
UMLS CUI [1,1]
C0342257
UMLS CUI [1,2]
C0205404
UMLS CUI [1,3]
C0332120
evidence of serious cardiovascular complications
Description

Cardiac complication Serious Evidence of

Type de données

boolean

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

Laboratory test result abnormal Significant

Type de données

boolean

Alias
UMLS CUI [1,1]
C0438215
UMLS CUI [1,2]
C0750502
other protocol-defined exclusion criteria may apply
Description

Exclusion Criteria Study Protocol

Type de données

boolean

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

Similar models

Eligibility Diabetes Mellitus, Type 2 NCT00101712

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])
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 22-45
boolean
C1305855 (UMLS CUI [1])
Non-Insulin-Dependent Diabetes Mellitus disease length
Item
diagnosis of type 2 diabetes for at least 8 weeks
boolean
C0011860 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
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])
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])
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])
Laboratory test result abnormal Significant
Item
significant laboratory abnormalities as defined by the protocol
boolean
C0438215 (UMLS CUI [1,1])
C0750502 (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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