ID

13134

Beschrijving

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

Link

https://clinicaltrials.gov/show/NCT00467168

Trefwoorden

  1. 19-01-16 19-01-16 -
Houder van rechten

CC BY-NC 3.0

Geüploaded op

19 januari 2016

DOI

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Licentie

Creative Commons BY-NC 3.0

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Eligibility Type 2 Diabetes Mellitus NCT00467168

Eligibility Type 2 Diabetes Mellitus NCT00467168

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 2 diabetes;
Beschrijving

type 2 diabetes

Datatype

boolean

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

antidiabetic agents

Datatype

boolean

Alias
UMLS CUI [1]
C0935929
nonsmokers;
Beschrijving

nonsmokers

Datatype

boolean

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

comorbidity

Datatype

boolean

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

gastro-enteral surgery

Datatype

boolean

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

dietary fat provided energy

Datatype

boolean

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

medications or vitamins known to affect plasma lipids

Datatype

boolean

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

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

Datatype

boolean

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

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
females with menstrual cycles
Beschrijving

females with menstrual cycles

Datatype

boolean

Alias
UMLS CUI [1]
C0279752

Similar models

Eligibility Type 2 Diabetes Mellitus NCT00467168

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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