Eligibility Type 2 Diabetes Mellitus NCT00467168

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 2 diabetes;
Description

type 2 diabetes

Data type

boolean

Alias
UMLS CUI [1]
C0011860
types and doses of antidiabetic agents had been unchanged for four weeks before the postprandial study;
Description

antidiabetic agents

Data type

boolean

Alias
UMLS CUI [1]
C0935929
nonsmokers;
Description

nonsmokers

Data type

boolean

Alias
UMLS CUI [1]
C0337672
no prior cardiovascular disease, hepatic and renal diseases, or other diseases influencing fat absorption;
Description

comorbidity

Data type

boolean

Alias
UMLS CUI [1]
C0009488
no previous history of gastro-enteral surgery;
Description

gastro-enteral surgery

Data type

boolean

Alias
UMLS CUI [1]
C0543467
dietary fat provided energy less than 35% in last two weeks;
Description

dietary fat provided energy

Data type

boolean

Alias
UMLS CUI [1]
C0012155
no use of medications or vitamins known to affect plasma lipids;
Description

medications or vitamins known to affect plasma lipids

Data type

boolean

Alias
UMLS CUI [1]
C1278073
ability to hold hypoglycemic drugs on the day of the study until postprandial tests are completed;
Description

ability to hold hypoglycemic drugs on the day of the study until postprandial tests are completed

Data type

boolean

Alias
UMLS CUI [1]
C0020616
ability to provide verbal informed consent to participate.
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
females with menstrual cycles
Description

females with menstrual cycles

Data type

boolean

Alias
UMLS CUI [1]
C0279752

Similar models

Eligibility Type 2 Diabetes Mellitus NCT00467168

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
type 2 diabetes
Item
type 2 diabetes;
boolean
C0011860 (UMLS CUI [1])
antidiabetic agents
Item
types and doses of antidiabetic agents had been unchanged for four weeks before the postprandial study;
boolean
C0935929 (UMLS CUI [1])
nonsmokers
Item
nonsmokers;
boolean
C0337672 (UMLS CUI [1])
comorbidity
Item
no prior cardiovascular disease, hepatic and renal diseases, or other diseases influencing fat absorption;
boolean
C0009488 (UMLS CUI [1])
gastro-enteral surgery
Item
no previous history of gastro-enteral surgery;
boolean
C0543467 (UMLS CUI [1])
dietary fat provided energy
Item
dietary fat provided energy less than 35% in last two weeks;
boolean
C0012155 (UMLS CUI [1])
medications or vitamins known to affect plasma lipids
Item
no use of medications or vitamins known to affect plasma lipids;
boolean
C1278073 (UMLS CUI [1])
ability to hold hypoglycemic drugs on the day of the study until postprandial tests are completed
Item
ability to hold hypoglycemic drugs on the day of the study until postprandial tests are completed;
boolean
C0020616 (UMLS CUI [1])
informed consent
Item
ability to provide verbal informed consent to participate.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
females with menstrual cycles
Item
females with menstrual cycles
boolean
C0279752 (UMLS CUI [1])