Eligibility Type 2 Diabetes Mellitus NCT01699932

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with type 2 diabetes mellitus inadequately controlled despite a treatment with sulfonylurea (su) alone or metformin alone or a free combination of su and metformin prior to the study entry.
Beskrivning

ID.1

Datatyp

boolean

signed informed consent, obtained prior any study procedure
Beskrivning

ID.2

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
age < legal age of adulthood
Beskrivning

ID.3

Datatyp

boolean

hba1c < 7% or ≥ 11%
Beskrivning

ID.4

Datatyp

boolean

bmi > 35 kg/m2
Beskrivning

ID.5

Datatyp

boolean

treatment with a stable dose of maximally tolerated su alone or metformin alone or the free combination of su and metformin for less than 12 weeks prior to the screening visit.
Beskrivning

ID.6

Datatyp

boolean

patients who received any anti-diabetic drug other than su or metformin within 12 weeks prior to the screening visit.
Beskrivning

ID.7

Datatyp

boolean

diabetes other than type 2 diabetes (e.g. type 1 diabetes, diabetes secondary to pancreatic disorders, drug or chemical agent intake…)
Beskrivning

ID.8

Datatyp

boolean

the above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Beskrivning

ID.9

Datatyp

boolean

Similar models

Eligibility Type 2 Diabetes Mellitus NCT01699932

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patients with type 2 diabetes mellitus inadequately controlled despite a treatment with sulfonylurea (su) alone or metformin alone or a free combination of su and metformin prior to the study entry.
boolean
ID.2
Item
signed informed consent, obtained prior any study procedure
boolean
Item Group
C0680251 (UMLS CUI)
ID.3
Item
age < legal age of adulthood
boolean
ID.4
Item
hba1c < 7% or ≥ 11%
boolean
ID.5
Item
bmi > 35 kg/m2
boolean
ID.6
Item
treatment with a stable dose of maximally tolerated su alone or metformin alone or the free combination of su and metformin for less than 12 weeks prior to the screening visit.
boolean
ID.7
Item
patients who received any anti-diabetic drug other than su or metformin within 12 weeks prior to the screening visit.
boolean
ID.8
Item
diabetes other than type 2 diabetes (e.g. type 1 diabetes, diabetes secondary to pancreatic disorders, drug or chemical agent intake…)
boolean
ID.9
Item
the above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
boolean