Eligibility Type 2 Diabetes NCT01072565

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female subjects ≥18 and ≤75 years of age
Beschreibung

ID.1

Datentyp

boolean

clinical diagnosis of diabetes
Beschreibung

ID.2

Datentyp

boolean

diabetes duration ≥ 1 year
Beschreibung

ID.3

Datentyp

boolean

hba1c ≥7.2%
Beschreibung

ID.4

Datentyp

boolean

diabetes can be treated with any therapy including medical nutrition therapy alone and any pharmaceutical therapy
Beschreibung

ID.5

Datentyp

boolean

Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
taken prednisone or cortisone medications in the previous 30 days
Beschreibung

ID.6

Datentyp

boolean

currently pregnant or planning pregnancy during the study period
Beschreibung

ID.7

Datentyp

boolean

presence of any severe medical or psychological condition or chronic conditions/infections that in the opinion of the investigator would compromise the subject's safety or successful participation in the study
Beschreibung

ID.8

Datentyp

boolean

unable to follow the study protocol
Beschreibung

ID.9

Datentyp

boolean

unable to speak, read and write in english
Beschreibung

ID.10

Datentyp

boolean

Ähnliche Modelle

Eligibility Type 2 Diabetes NCT01072565

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
male or female subjects ≥18 and ≤75 years of age
boolean
ID.2
Item
clinical diagnosis of diabetes
boolean
ID.3
Item
diabetes duration ≥ 1 year
boolean
ID.4
Item
hba1c ≥7.2%
boolean
ID.5
Item
diabetes can be treated with any therapy including medical nutrition therapy alone and any pharmaceutical therapy
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
taken prednisone or cortisone medications in the previous 30 days
boolean
ID.7
Item
currently pregnant or planning pregnancy during the study period
boolean
ID.8
Item
presence of any severe medical or psychological condition or chronic conditions/infections that in the opinion of the investigator would compromise the subject's safety or successful participation in the study
boolean
ID.9
Item
unable to follow the study protocol
boolean
ID.10
Item
unable to speak, read and write in english
boolean