Eligibility Diabetes Mellitus, Type 2 NCT00349986

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 2 diabetes mellitus
Beschreibung

Diabetes Mellitus, Non-Insulin-Dependent

Datentyp

boolean

Alias
UMLS CUI [1]
C0011860
insufficient combined oral antidiabetic treatment (biguanide + sulfonylurea)
Beschreibung

Antidiabetics Oral Combined Insufficient | Biguanides | Sulfonylurea

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0935929
UMLS CUI [1,2]
C1527415
UMLS CUI [1,3]
C0205195
UMLS CUI [1,4]
C0231180
UMLS CUI [2]
C0005382
UMLS CUI [3]
C0038766
bmi >25 kg/m2 , <30 kg/m2
Beschreibung

Body mass index

Datentyp

boolean

Alias
UMLS CUI [1]
C1305855
hba1c value >7.0%, <9.0% within one month
Beschreibung

Glycosylated hemoglobin A Percentage

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0019018
UMLS CUI [1,2]
C0439165
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
type 1 diabetes mellitus
Beschreibung

Diabetes Mellitus, Insulin-Dependent

Datentyp

boolean

Alias
UMLS CUI [1]
C0011854
known malignancy
Beschreibung

Malignant Neoplasms

Datentyp

boolean

Alias
UMLS CUI [1]
C0006826
drug or alcohol abuse
Beschreibung

Substance Use Disorders

Datentyp

boolean

Alias
UMLS CUI [1]
C0038586
severe liver disease
Beschreibung

Liver disease Severe

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0023895
UMLS CUI [1,2]
C0205082
renal failure (se creatinine > 150 micro mol/l)
Beschreibung

Kidney Failure | Creatinine measurement, serum

Datentyp

boolean

Alias
UMLS CUI [1]
C0035078
UMLS CUI [2]
C0201976
the above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Beschreibung

Study Subject Participation Status

Datentyp

boolean

Alias
UMLS CUI [1]
C2348568

Ähnliche Modelle

Eligibility Diabetes Mellitus, Type 2 NCT00349986

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus, Non-Insulin-Dependent
Item
type 2 diabetes mellitus
boolean
C0011860 (UMLS CUI [1])
Antidiabetics Oral Combined Insufficient | Biguanides | Sulfonylurea
Item
insufficient combined oral antidiabetic treatment (biguanide + sulfonylurea)
boolean
C0935929 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
C0205195 (UMLS CUI [1,3])
C0231180 (UMLS CUI [1,4])
C0005382 (UMLS CUI [2])
C0038766 (UMLS CUI [3])
Body mass index
Item
bmi >25 kg/m2 , <30 kg/m2
boolean
C1305855 (UMLS CUI [1])
Glycosylated hemoglobin A Percentage
Item
hba1c value >7.0%, <9.0% within one month
boolean
C0019018 (UMLS CUI [1,1])
C0439165 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Diabetes Mellitus, Insulin-Dependent
Item
type 1 diabetes mellitus
boolean
C0011854 (UMLS CUI [1])
Malignant Neoplasms
Item
known malignancy
boolean
C0006826 (UMLS CUI [1])
Substance Use Disorders
Item
drug or alcohol abuse
boolean
C0038586 (UMLS CUI [1])
Liver disease Severe
Item
severe liver disease
boolean
C0023895 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Kidney Failure | Creatinine measurement, serum
Item
renal failure (se creatinine > 150 micro mol/l)
boolean
C0035078 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
Study Subject Participation Status
Item
the above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
boolean
C2348568 (UMLS CUI [1])