ID

13134

Description

Optimal Dietary Fat Pattern to Prevent Cardiovascular Disease Among Type 2 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT00467168

Lien

https://clinicaltrials.gov/show/NCT00467168

Mots-clés

  1. 19/01/2016 19/01/2016 -
Détendeur de droits

CC BY-NC 3.0

Téléchargé le

19 janvier 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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Eligibility Type 2 Diabetes Mellitus NCT00467168

Eligibility Type 2 Diabetes Mellitus NCT00467168

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 2 diabetes;
Description

type 2 diabetes

Type de données

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

Type de données

boolean

Alias
UMLS CUI [1]
C0935929
nonsmokers;
Description

nonsmokers

Type de données

boolean

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

comorbidity

Type de données

boolean

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

gastro-enteral surgery

Type de données

boolean

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

dietary fat provided energy

Type de données

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

Type de données

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

Type de données

boolean

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

informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
females with menstrual cycles
Description

females with menstrual cycles

Type de données

boolean

Alias
UMLS CUI [1]
C0279752

Similar models

Eligibility Type 2 Diabetes Mellitus NCT00467168

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])

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