Eligibility Diabetes Mellitus Type 2 NCT01510522

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
diabetes mellitus type 2 diagnosed (baseline glycemia > 7,0 mmol/l (126 mg/dl) or overload glycemia > 11,0 mmol/l (198 mg/dl)
Descrição

ID.1

Tipo de dados

boolean

on treatment with metformin tablets
Descrição

ID.2

Tipo de dados

boolean

patients with at least 2 treated co-morbidities
Descrição

ID.3

Tipo de dados

boolean

established dose of metformin > 1.700 mg/day
Descrição

ID.4

Tipo de dados

boolean

age > 18 years old
Descrição

ID.5

Tipo de dados

boolean

given informed consent
Descrição

ID.6

Tipo de dados

boolean

Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients not able to take medication orally
Descrição

ID.7

Tipo de dados

boolean

according to summary of product characteristics (smpc)
Descrição

ID.8

Tipo de dados

boolean

participating in another clinical trial 30 days prior to randomization
Descrição

ID.9

Tipo de dados

boolean

any other illness or medical or psychiatric condition, severe and uncontrolled that could interfere in the patient's participation or in the assessment of the study results
Descrição

ID.10

Tipo de dados

boolean

Similar models

Eligibility Diabetes Mellitus Type 2 NCT01510522

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
diabetes mellitus type 2 diagnosed (baseline glycemia > 7,0 mmol/l (126 mg/dl) or overload glycemia > 11,0 mmol/l (198 mg/dl)
boolean
ID.2
Item
on treatment with metformin tablets
boolean
ID.3
Item
patients with at least 2 treated co-morbidities
boolean
ID.4
Item
established dose of metformin > 1.700 mg/day
boolean
ID.5
Item
age > 18 years old
boolean
ID.6
Item
given informed consent
boolean
Item Group
C0680251 (UMLS CUI)
ID.7
Item
patients not able to take medication orally
boolean
ID.8
Item
according to summary of product characteristics (smpc)
boolean
ID.9
Item
participating in another clinical trial 30 days prior to randomization
boolean
ID.10
Item
any other illness or medical or psychiatric condition, severe and uncontrolled that could interfere in the patient's participation or in the assessment of the study results
boolean